Compensation for Bad Blood

2006-10-31 22:09:22

Compensation for Bad Blood
Tories poised to unveil new funding
OTTAWA -- The federal government is close to announcing a compensation package
for the "forgotten victims" of tainted blood, sources say.
Approximately 5,500 people who were infected with hepatitis C before 1986 or
after 1990 are expected to receive substantial payments under the deal.
Funding could be in the same range as the original $1.1-billion
federal-provincial package announced in 1998, said one source, speaking on
condition of anonymity.
The original deal was restricted to people infected between 1986 and 1990, since
the government of the day claimed it could have done nothing to prevent
infections outside that period.
That argument was refuted as documents surfaced showing that screening tests
available before 1986 could have prevented many, if not most, of the infections.
In opposition, the Conservatives pressed the government to provide equal
compensation for all victims, regardless of when they were infected. The new
package is expected to give the excluded victims at least as much as those in
the 1986-1990 group.
"I think we'll probably have good news within the next week or so," said a
source in the hepatitis C community, who praised the Conservative government for
moving on the issue.
"They've really done their job this time. I want to give them kudos for working
diligently to ensure we're going to get help to people."
A $3.8-billion class-action lawsuit against the federal government will be
dropped when the package is announced, said the source.
Unlike the 1998 compensation package, there is no provincial participation.
Legal action is expected to continue against some provinces that have not
compensated all victims.
The new fund will be structured differently from the 1998 deal, which resulted
in much of the money going to legal fees.
Other fallout from the tainted-blood scandal will continue, including criminal
trials of officials involved in managing the blood system, and a $1-billion suit
over the distribution of contaminated blood from an Arkansas prison.
An RCMP investigation into the Arkansas blood is also continuing.
http://www.edmontonsun.com/News/Canada/2006/06/03/1612749-sun.html

Treating Obesity May Improve The Efficacy Of Therapy For Hepatitis C

2006-10-31 21:47:46

Treating Obesity May Improve The Efficacy Of Therapy For Hepatitis C
Article Date: 03 Jun 2006 - 0:00am (PDT)
According to a new study, obese patients chronically infected with the hepatitis
C virus (HCV) and treated with combination drug therapy may have better outcomes
if the underlying abnormalities caused by excessive fat tissue are corrected.
Weight loss, medications to decrease insulin resistance and extending duration
or dosage of therapy are strategies that may improve the efficacy of therapy.
The results of this study appear in the June 2006 issue of Hepatology, the
official journal of the American Association for the Study of Liver Diseases
(AASLD). Published by John Wiley & Sons, Inc., Hepatology is available online
via Wiley InterScience at http://www.interscience.wiley.com/journal/hepatology.
HCV is one of the leading causes of chronic liver disease worldwide, affecting 3
percent of the world's population. In the U.S. alone 4.1 million people have
been infected with HCV, and up to 85 percent of those are chronic carriers of
the virus. Up to 70 percent of chronic carriers will go on to develop some other
form of chronic liver disease, from mild liver enzyme abnormalities to cirrhosis
and liver cancer. While there is no vaccine for HCV, the current optimal
treatment is combination therapy with peginterferon alfa (an immune stimulant)
and ribavirin (an inhibitor of viral replication). However, this will cure only
55 percent of patients. One of the risk factors for treatment failure is
obesity.
Obesity itself is linked to the disruption of hormone signaling pathways that
affect cell function and to abnormal levels of circulating proteins and sugars.
In other words, obesity is associated with a wide range of metabolic changes
that affect multiple cellular and organ functions. This biochemical
disregulation is linked to serious chronic medical conditions, such as heart
disease, diabetes, and non-alcoholic fatty liver disease.
Given the association between obesity and metabolic abnormalities, Michael R.
Charlton, M.D. of the Division of Gastroenterology and Hepatology at the Mayo
Clinic and Foundation in Rochester, MN and coauthors reviewed several mechanisms
by which obesity may interfere with the treatment of chronic HCV and recommend
management strategies for obese patients.
The authors identify three possible ways by which obesity may interfere with
peginterferon alpha and ribavirin activity. First, fat tissue actively secretes
hormones that can modulate the immune system. Increases in fat tissue may
disregulate immune pathways peginterferon targets, rendering the drug
ineffective. Second, obesity causes insulin resistance which itself leads to the
accumulation of fat in the liver. The greater the accumulation of fat in the
liver, the greater the risk of fibrosis, or scar tissue formation, that alters
liver function and blood flow, often permanently. Because HCV also causes liver
cells to not respond to insulin, obesity may simply compound the problem and
worsen liver disease. Third, fat tissue reduces the amount of peginterferon
circulating in the body. The decreased circulation of the drug may also weaken
peginterferon's stimulation of the immune system against HCV.
To address all of these mechanisms, the authors make three treatment
recommendations. First, weight loss to reduce fat tissue would address all three
hypothesized mechanisms. Weight loss in obese HCV patients is already associated
with improved liver biopsy results and liver enzyme levels. Second, treatment
with drugs that improve cellular sensitivity to insulin, such as the diabetes
drugs metformin or pioglitazone, would lead to reduced fat accumulation in liver
cells and might reverse disease progression. Third, increasing the dosages or
the duration of combination therapy may increase circulating drug levels and
improve drug efficacy.
"Treatment strategies that focus on improving underlying metabolic factors
associated with poor response to combination therapy are thus more likely to
overcome the low sustained viral response rates often observed in obese patients
infected with HCV," conclude the authors.
David Greenberg
dgreenbe@...
John Wiley & Sons, Inc.
http://www.interscience.wiley.com/
http://www.medicalnewstoday.com/medicalnews.php?newsid=44470&nfid=rssfeeds

failure of treatment

2006-10-31 06:36:33

Well I have now sucessfuly fail treatment three times. Oh well
thats the way it goes sometimes. I hope to last long enough to have
the new vertex950. best wishes to all.

Clarification

2006-10-31 06:24:47

Just some quick clarification in case some are getting confused. SSI is
Supplemental Security Income and is different than SSDI which is Social Security
Disability Income. Two years from the date you are found disabled with SSDI
you get Medicare (not Medicaid). A lawyer is a very good idea as it is very
hard to get SSDI without one (although a few have) It is also hard to get
SSDI based on just Hep C. Most of us have more wrong with us anyway. If you
are working and applying for disability it is doubtful you will ever get it.
The purpose of disability is for when you can't work. If you are working they
will expect you to continue doing so. I suggest finding a job that pays cash if
you need $$ to survive on while you are waiting and find supportive friends
and/or family members to move in with. If you have no income you are eligible
for SSI but it pays very little each month. Something like $400 a few years
ago.... might be a tad more now. Your SSDI income is based on how much you
paid INTO the system during the years that you worked. That is why everyone's
SSDI income varies so much. Some people get a great deal more money every
month than others. I suggest that those of you who are just starting with *the
system* go to www.ssa.gov/ and read and read and read ;-) Keep applying and
reapplying. They hope that you give up and go away ;-) GOOD LUCK!
Peace
Pam
BTW....... the online Blue Book for disabilities can be found at:
http://www.ssa.gov/disability/professionals/bluebook/
The gastro section is at:
http://www.ssa.gov/disability/professionals/bluebook/5.00-Digestive-Adult.htm
with Hepatitis being under 5.05 You used to need at least TWO things wrong
with you from this section
These and many other links can be found at http://www.HEALSofNFL.bravehost.com
1/2 way down the page. Look for the link that says Excellent fatigue, fibro,
Hepatitis, and SSDI info.

Re: failure of treatment

2006-10-30 20:09:08

Smithy,
You have not failed treatment....the treatment failed you!!
Glenn

Treatment and SSDI misconceptions

2006-10-30 15:25:49

Amen to that Glenn! I am sorry to hear that the treatment failed YOU Smithy.
Hang in there. 50% of us are in the same boat.
I have heard some good things about VX-950 from a dinner I went to that had a
Doc speaking. It is added TO interferon (and most of the time Riba too) He
said there would not be anything that didn't need interferon for at least 8 to
10 years. He thinks two protease inhibitors will be approved by late next year
with the VX-950 showing the most promising results right now. The polymerase
inhibitors are not looking as promising. He also talked a little about the
Alinia that I posted about a few days ago. It is already FDA approved but not
for Hep C yet.

AIDS AT 25

2006-10-30 12:30:23

AIDS AT 25
Sabin Russell, Chronicle Medical Writer
Sunday, June 4, 2006
On June 5, 1981, Dr. Michael Gottlieb, a young immunologist at the UCLA School
of Medicine, reported five cases of a rare pneumonia among gay men in Los
Angeles. Each had a profoundly depressed immune system. Two were already dead.
His report in the weekly bulletin of the Centers for Disease Control was the
first medical description of what would come to be known as acquired immune
deficiency syndrome. It signaled the start of a global scourge that has since
killed 25 million. Today, a quarter-century later, it is estimated that 38.6
million people are living with HIV, the virus that causes AIDS.
Gottlieb had no idea that he had discovered a monster. "I thought this might be
bigger than Legionnaire's disease," he recalled, referring to the discovery five
years earlier of a previously unknown bacterium that killed 29 attendees at an
American Legion convention in Philadelphia.
Soon after Gottlieb's paper appeared, similar accounts of Pneumocystis carinii
pneumonia were trickling in from gay neighborhoods in New York and San
Francisco. Those new reports also described outbreaks among gay men of Kaposi's
sarcoma, a rare skin cancer that caused disfiguring purple lesions.
Amid the initial excitement of medical researchers on the trail of a new
disease, no one knew that 250,000 gay men in the United States were already
infected with HIV.
Twenty-five years later, the world is still playing catch-up. One million
Americans are living with HIV, but 25 percent of them do not know it. Worldwide,
9 out of 10 people carrying the virus have yet to be tested, according to
estimates from UNAIDS, the United Nations program on HIV/AIDS.
The hidden toll is a grim tribute to the insidious nature of the human
immunodeficiency virus. A tiny package of just nine genes, HIV is a lentivirus,
or slow virus, that gradually degrades the immune system, leaving the body
vulnerable to fatal assaults from bacteria and other viruses. HIV can leave a
person healthy for 10 years, free to spread it to others through sex or
contaminated needles.
It was in San Francisco's bacchanalian gay culture of the early 1980s that the
virus fully demonstrated its capacity for chaos - silently infecting close to
half that community with a fatal, sexually transmitted disease.
As scientists and doctors struggled to understand what was happening, the
unidentified virus raced ahead. In 1982 and 1983, the infection rate within San
Francisco's gay population was increasing at an astonishing 18 percent per year.
Since those first puzzling cases, at least 18,000 people in San Francisco have
died of the disease - six times the estimated toll of the earthquake and fire
100 years ago.
Like most natural catastrophes, AIDS brought out the best and worst of human
nature.
"I saw incredible heroism," said Dr. Marcus Conant, a San Francisco
dermatologist who encountered some of the earliest Kaposi's sarcoma cases. " I
saw hundreds of gay men who stayed with their partners and watched their loved
ones die horribly, knowing they faced the same death in a matter of months."
But Conant also encountered ugliness within his own profession, in his own city.
"There were a lot of doctors who did not want 'those kind of patients' in their
waiting rooms," he said.
A disease that first emerged among marginalized groups - homosexual men,
prostitutes and injection-drug users - AIDS exploited social stigma wherever it
emerged. Instead of sympathy, AIDS often aroused contempt; instead of
compassionate care, it encouraged fear and neglect.
"This is the most political disease I have ever seen," said Dr. Mervyn
Silverman, who was director of the San Francisco health department when AIDS
emerged in 1981. The city's signature encounter with AIDS in the 1980s would be
replayed elsewhere, again and again, as the virus spread around the globe.
"It is deja vu every time it hits a new country," said Dr. Anthony Fauci,
director of the National Institutes of Allergy and Infectious Diseases. "First
it is denial: 'Nothing is happening.' Then it's 'someone else's problem.' Then
it is, 'Oh my God, help us " Today, entire countries in southern Africa are
facing infection rates like those endured in San Francisco's Castro
neighborhood. In Botswana and Swaziland, at least a quarter of adults are living
with HIV.
It took the medical world an even longer time to wake up to AIDS in Africa,
where the epidemic had been smoldering for decades. New York AIDS researcher Dr.
David Ho would eventually find HIV in a sample of blood from a patient in 1959
in what was then called the Belgian Congo.
European researchers had clues of the disease during the 1970s in a spate of
unexplained illnesses among Africans living in Europe.
In October 1983, Dr. Peter Piot, a Belgian tropical-disease specialist who had
seen some of those early European cases, led a team of researchers to the
Congolese capital, Kinshasa. At the Mamma Yemo Hospital, he saw wards packed
with emaciated, dying women.
"I knew this was really bad news," he said. "It looked like AIDS. We had
something heterosexual going on there."
A heterosexual AIDS epidemic was, in fact, exploding in Africa. It followed
soldiers in the bloody conflicts of the region, and along the trucking routes,
where prostitutes serviced long-distance haulers. It spread to remote mining
camps and squalid urban slums - where male laborers from rural villages worked
for months, had sex with infected prostitutes and girlfriends, and then returned
home to their wives.
When apartheid fell in South Africa in 1994, the previously isolated nation
opened its borders to the rest of Africa, and AIDS walked in, too. Last year,
5.5 million South Africans - including 1 in 5 adults - were believed to be
HIVpositive.
Piot eventually would be named executive director of UNAIDS. The agency
estimates today that there are 24.5 million people living with HIV in sub-
Saharan Africa. In 2005, the latest year for which statistics are available, the
region logged 2.7 million new infections, and 2 million men, women and children
died there of AIDS.
While AIDS roared unfettered through Africa, strategies to combat the pestilence
were evolving in the United States.
A new HIV test protected the nation's blood supply. San Francisco's gay men
dramatically altered their sexual behavior. They used condoms, reduced their
number of sex partners and avoided the most dangerous practices such as
unprotected receptive anal intercourse.
Infection rates plummeted. A grassroots network of volunteer organizations
melded with city and university clinics to provide the sick and dying with care.
This "San Francisco model" was duplicated across the country and around the
world.
Epidemiologists experimented with needle-exchange programs to protect
injection-drug users. Activists battled for the rights of the infected, for
government aid and for a cure.
"AIDS has been a crucible that tested everybody," said Martin Delaney, a
business consultant who founded San Francisco's Project Inform in 1985. "Out of
that furnace came a new model of medical care and for funding research for the
development of drugs."
Still, the virus continued to race ahead of its pursuers. AZT, the first AIDS
antiviral, was approved by the Food and Drug Administration in 1987. But doctors
soon learned that the virus could quickly develop resistance to it.
Activists pushed the FDA for speedier approval of experimental medicines. With
each new drug, patients bought time for the day when something that really
worked might come along. That day came in the summer of 1996.
At the 11th International AIDS Conference in Vancouver, British Columbia,
scientists delivered the news that three-drug combinations of newly developed
antiviral drugs - particularly those using a new class called protease
inhibitors - could tame the relentless killer. Death rates in Western nations
that could afford the medicines soon fell by more than half.
"We'd literally see people recover miraculously with these rugs," said Dr. Paul
Volberding, who ran the renowned AIDS program at San Francisco General Hospital.
At the time, the new triple-drug regimes were called "cocktails." Today, the
common word is an acronym - HAART - for highly active antiretroviral therapy.
There are 27 distinct antiviral drugs or combinations sold in the United States
today.
For wealthy Western countries, HAART transformed the epidemic.
"I'll probably die from a heart attack or any of the various things that run in
my family," said Bob Katz, 55, a real estate appraiser in San Francisco who has
been infected with HIV for 25 years.
Yet early hope that HAART could eradicate the virus was misplaced. Patients
still developed drug resistance, and latent pools of infected cells allow HIV to
roar back when medicines are stopped.
Side effects such as lipodystrophy - the destruction of fat tissue in the face
and arms - have created a new face of AIDS: the hollowed cheeks of many patients
on HAART. There are lingering fears that the long-term price of AIDS drugs may
be cancer.
AIDS drug cocktails were nevertheless a reprieve for thousands and have
transformed HIV in developed nations from a death sentence into a chronic
medical condition.
Ross Woodall's life was saved by the drugs. In 1987, his doctor gave him six
months to live. The former travel agency vice president watched his friends die
by the dozens, but he weathered bouts of illness from bugs that exploited his
ruined immune system.
He eventually lost 95 pounds. He burned through every antiviral medicine that
came on the market. In 1998, the combination therapy turned his health around.
But side effects from years of antiviral medications have drained the fat from
his face and limbs, and he is legally blind from an AIDSrelated viral infection.
At the age of 53, Woodall remains upbeat. He works part time as a travel agent
and volunteers for AIDS prevention and care programs.
"I've been to hell and back," he said. "If I can keep someone else from going
there, I'd like to do that."
Although modern medicine in the United States has caught up with HIV, the virus
maintains its edge in much of the rest of the world because the drugs that saved
lives here remain out of reach for the overwhelming majority of people living
with AIDS. They are just too expensive. Yet there are signs of hope.
Driven by political activists demanding drugs for the poor, and by Indian
pharmaceutical companies that could make the new pills for less than a dollar a
day, a global movement for universal treatment of HIV took wing in 2000. Generic
drugmakers could copy Western AIDS medicines without having to recoup research,
development and marketing costs. They could sidestep Western patent law. They
put AIDS drugs within reach, if the West would only subsidize the cost.
Politicians took note.
Since it was founded in 2002, the nonprofit, U.N.-inspired organization Global
Fund to Fight AIDS, Tuberculosis and Malaria has provided $2 billion in
assistance, and in 2003 President Bush began his own $15 billion overseas
AIDS-relief effort.
Today, 1 million of the 6 million AIDS patients in the developing world who need
antiviral drugs are taking them. The push for treatment has created for the
first time an incentive for Africans to be tested for the illness. Studies show
that once people know they are HIV-positive, they are less likely to spread the
virus.
"For the first time in a quarter-century," said Piot, the UNAIDS executive
director, "we are in a position to get ahead of this epidemic. But it is going
to require an enormous and sustained effort."
Despite these signs, there is no vaccine and no cure. Safer-sex behaviors have
proved difficult to sustain. Ominously, in the United States, the disease is
burrowing into impoverished neighborhoods and disproportionately affecting
blacks. The CDC estimates that 40,000 new infections occur in the United States
each year, and increasingly they are occurring among blacks and women.
Today, the harder edges of the local AIDS epidemic can be found in San
Francisco's homeless population. "It's still a mortal illness in the
Tenderloin," said Alexandra Monk, project coordinator for REACH - Research into
Access to Care for the Homeless. "We've lost over 100 in the last four years."
DeShawn Patton, 41, said she has been HIV-positive for two decades. She lives in
a small and crowded hotel room off O'Farrell Street with her boyfriend of six
years, who is HIV-positive and has cancer.
Patton was born male, and grew up a gay teenager. Today, she lives her life
fully as a woman. "The hardest thing for my family is not that I have AIDS but
accepting me as transgender," she said.
Patton's health has been slipping. Her T-cell count - a measure of
infection-fighting white blood cells, has dipped to 119 - a healthy number is
600 or more. She had a bout with pneumonia that sent her to San Francisco
General Hospital, but she bounced back, as she has all her life.
Around her, HIV still has a grip on the community in ways once seen in the 1980s
in the upscale Castro, just a few miles up Market Street.
In the Tenderloin, sickness and death rates are higher because of the nature of
life on the street, of substance abuse, poor diet, hepatitis C and untreated
mental illness. Blood tests of the poor and homeless in the Tenderloin show that
at least 11 percent of that population is infected with HIV - a higher rate than
in Uganda, where the same UCSF researchers run an AIDS treatment clinic.
Dr. Brad Hare, medical director of the Positive Health Program at San Francisco
General Hospital, is Patton's physician. When the AIDS epidemic was first
described 25 years ago, Hare, 36, was in elementary school.
Hare was a medical student at Duke when he saw his first AIDS patient, a New
York artist who had moved back to North Carolina to die. When the patient
recovered under treatment with the new AIDS drugs, Hare was hooked. "That's why
I went into medicine," he said.
Half the patients he treats at San Francisco General today are black or Latino.
They are often poor, living in ramshackle housing or in the streets, and they
are very sick.
"We still see people come into our hospital for their first test for HIV, and
they have pneumocystis pneumonia, cryptococcal meningitis and 10 Tcells," Hare
said. "We still see people die of classic, old-fashioned AIDS."

Our Sisters

2006-10-30 06:11:43

Wish I could offer 'good' answers, I wish your better times and pray for 'Your
best'!

Liver link in heroin deaths

2006-10-29 23:08:10

Liver link in heroin deaths
Harriet Alexander
June 5, 2006
THE mystery of long-term heroin users dying by overdose despite experience with
the drug may have been solved by a study linking overdoses with liver disease.
Researchers have puzzled for years about why heroin users defy the laws of
experience and mortality that apply to others who practise risky activities -
the older and wilier you become, the more likely you are to survive.
Instead, heroin overdoses are more likely to occur among people who have used
the drug in a similar way for many years.
The NSW Drug and Alcohol Research Council investigated 841 deaths caused by
opioid toxicity and found a 10th of those aged 35 to 44 and a quarter of those
older than 44 had been diagnosed with cirrhosis.
This could make them more susceptible to overdose, said Professor Shane Darke,
of the Drug and Alcohol Research Council at the University of NSW.
"They've got these phenomenally high rates of . liver disease," Dr Darke said.
"If they hadn't died of overdose, they would have died of cirrhosis."
A 70 per cent incidence of hepatitis C and a high rate of alcohol consumption
may account for the likelihood of liver disease, the study said. Nearly a
quarter of those studied had multiple-organ disease. "They're drinking, they're
using heroin frequently, their bodies are just wearing out," Dr Darke said.
The council's information manager, Paul Dillon, said the study confirmed the
importance of getting young users into early treatment. "The trouble is,
treatment is not particularly attractive to young people," Mr Dillon said. "And
you see these [problems] 15 years down the track."
The latest figures show that 357 Australians died of heroin and opioid overdose
in 2004. Those aged 25-34 comprised the biggest group at 43 per cent, followed
by people aged 35 to 44 (28 per cent), 45 to 54 (18 per cent) and 15 to 24 (10
per cent).
http://www.smh.com.au/news/national/liver-link-in-heroin-deaths/2006/06/04/11493\
59612894.html

RE: [HepCingles2] failure of treatment

2006-10-29 13:44:34

Smithy,
Don't feel alone. I failed treatment, or it failed me, after doing treatment for
18 straight months, three times a week, 1 million units per shot.
Back when I did treatment, I was just known as non-A, non B
Interferon was a night mare, but it because even worse, when after all that
time.
I was not only non-responsive, but it took out my platelets, white and red cell
count.
Making me ineligible for any more treatment.
I am now trying to make the list as a transplant patient.
Weather I make it or not, is not an issue.
The issue is, I've tried all that is available.
I am geno type 1a stage 4, meld score 13
Keep your chin up.
Sincerely
Doreen

Recovering addict's new test: Hepatitis C

2006-10-29 10:06:32

Recovering addict's new test: Hepatitis C
By Dorsey Griffith -- Bee Medical Writer
Published 12:01 am PDT Sunday, June 4, 2006
It's been three years since Kristina Taylor tried to end it all, asking two men
to unload full syringes of methamphetamine into her arms simultaneously. And
it's been eight months since she's taken a drop of alcohol.
Now, clean and sober, the 38-year-old Rancho Cordova woman wants to slay a
different beast, one that has her in the grip of another fight for her life:
liver disease caused by hepatitis C.
"I don't want to die no more," Taylor says. "I want to live."
Although the sometimes fatal viral illness is rampant -- affecting more than
25,000 people in Sacramento County alone -- its treatment has been unattainable
for most, especially those most vulnerable to the disease: low-income men and
women with a history of injection drug use.
"Very few people are willing to undertake these cases," explained Dr. Diana
Sylvestre, the gutsy executive director of the O.A.S.I.S. Clinic in Oakland,
which provides care to hundreds of patients with addiction, hepatitis C and
other health problems. "They are very challenging patients."
By taking on the difficult cases, holding rallies, hounding legislators for
support and educating anyone who will listen, Sylvestre and a growing cadre of
activists are working to fill the void. Their goal: to stanch an epidemic that
affects an estimated 4 million to 5 million Americans and kills about 8,000 of
them every year.
"The working principle is that all patients with hepatitis C are potential
candidates for therapy," said Barbara Sigler, a nurse practitioner with the
California Pacific Medical Center in San Francisco.
Sigler is one of several medical specialists who is training front-line nurses
and doctors determined to confront hepatitis C -- and all the complications that
go with it.
Her audience on a recent Tuesday was a Sacramento group that calls itself Moving
Mountains, aptly named for medical practitioners from the region who have
decided to join the uphill battle against the disease.
Fortunately, Sigler explained, new drug combinations -- pegylated interferon and
ribavirin -- can eliminate the virus in 50 percent to 80 percent of those
treated, depending on the type of hepatitis C and the patients' genetic makeup.
But there are caveats. As Sigler said, the drugs -- daily pills and weekly
injections taken for up to 18 months -- can produce miserable side effects.
Among them: fatigue, depression, headache, anemia, fever, anxiety, nausea,
heartburn, loss of appetite, hair loss, gastric reflux disease and itching.
"One of our patients recently waved a gun around in his neighborhood and was
arrested," Sigler told the group. "We've had two suicides. One drank herself to
death."
About 40 percent of Sacramento County's indigent adults are infected with
hepatitis C, which is spread through contact with infected blood.
In just a couple of weeks recently, county staff compiled a list of 80 patients
who tested positive for the virus and were interested in treatment, said Dr.
Dorothy Pitman, county clinics director.
But finding a gastroenterologist -- much less one who specializes in liver
disease -- can be an exercise in frustration. Waiting times can last as long as
a year, she said.
"They all believe they are going to die," Pitman said. "Then, when they are put
on waiting lists or told there is no treatment, it is very discouraging."
Part of the problem is that many people with hepatitis C also struggle with drug
or alcohol addiction or other ailments, such as mental illness, making their
treatment even more complex.
The rate of new hepatitis C infections actually has dropped in recent years
because blood banks screen for the virus and because drug users are more aware
of the hazards of needle-sharing.
Nevertheless, the need for medical care has never been more acute. That's
because people who became infected decades ago -- many from experimental drug
use -- only now are beginning to get sick.
Hepatitis C can wreak havoc on the liver for years before it's detected, said
Dr. John Vierling, a liver specialist at Baylor College of Medicine.
"The death rate is increasing, rates of liver (cirrhosis) and liver cancer are
increasing," said Vierling, president of the American Association for the Study
of Liver Diseases. "Hepatitis C-cirrhosis is the leading indication for liver
transplants in the United States."
Sacramento County held its first hepatitis C clinic last month. Nineteen
patients assembled at Sacramento County's Primary Care Center on Stockton
Boulevard.
"Everyone in here has a different story," said Pitman, the county clinics
director. "Not everybody will be a good candidate for treatment."
After viewing videos aimed at busting hepatitis C myths, patients asked their
own questions:
"Will I have to have a biopsy before treatment?" asked one.
"Can I get treatment while I'm taking narcotic drugs for pain?" asked another.
"If I bleed into the food I am preparing, can I infect someone?" wondered
another.
Taylor asked if her 10-year-old daughter, who was born with antibodies to
hepatitis C, actually has the disease itself.
Pitman explained that 20 percent of children exposed to the virus at birth will
fight off the infection on their own.
Later, in an exam room with Pitman, Taylor described how she regularly injected
methamphetamine in her early 20s, how she has been treated for mental illness
and how she once tried to kill herself with an overdose, distraught over her
father's death and loss of custody of her two children.
"I'm ready," she said of her drive to treat her disease. "I want to get better."
Pitman reviewed Taylor's medical chart, noting high blood sugar levels and signs
of liver disease from previous blood tests.
Treatment for hepatitis C, Pitman told her, "is no walk in the park." The drugs
can exacerbate depression, so controlling the mental illness is essential before
starting medication.
"They say I have cirrhosis," Taylor said, her eyes filling with tears. "They say
my liver is a cobblestone."
Sacramento County's outreach to indigent adults with hepatitis C represents part
of a fledgling national movement to tackle the problem early, from the trenches
of medicine.
The federal Department of Veterans Affairs has led the way, and other medical
personnel dedicated to society's disenfranchised now are taking on the emerging
epidemic.
The National Association of Community Health Centers, for example, launched
pilot projects last year that trained providers in six clinics to treat
hepatitis C. In just nine months, more than 800 cases were detected.
UC Davis liver specialist Lorenzo Rossaro, who works with Sacramento County
providers treating hepatitis C patients, also consults electronically with
doctors at 65 clinics throughout Northern California.
And, starting in July, the Bi-Valley Medical Clinics in Sacramento County, which
provide methadone treatment for heroin and other opiate addicts, will begin
treating hepatitis C.
Bi-Valley program director Garrett Stenson said hepatitis C is the leading cause
of death among his patients. Yet many are refused medical treatment for the
disease, even after kicking heroin addiction.
"We are sick of watching our patients die," Stenson said.
Of the first 19 hepatitis C patients who came through the county primary care
clinic, nine were deemed good candidates for therapy and will return later this
month to get started.
Pitman said a blood test proved that one patient no longer had the virus; eight
others will be re-evaluated periodically for possible treatment down the line.
Two weeks after her first visit, Taylor returned to the clinic feeling both
giddy and anxious.
The news was mixed. Taylor let out a whoop upon learning that she is not
diabetic. But she winced when Pitman told her that tests showed low supplies of
white blood cells and platelets due to her liver disease. Treatment for
hepatitis C, which can by itself cause anemia, could worsen that condition, she
said.
"We have a gastroenterologist at UCD who is helping us," Pitman said, referring
to Rossaro. "I want to talk to him about your treatment. I'm not comfortable
proceeding ahead."
Psychiatrist John Onate added that Taylor needs to understand that hepatitis C
drug treatment also could worsen her mental state.
"I'm going to have a strong will about me," Taylor assured him. "I'll tell
myself every day, 'This is for the good.' "
About the writer:
a.. The Bee's Dorsey Griffith can be reached at (916) 321-1089 or
dgriffith@....
Hepatitis C links
Hepatitis Foundation International: www.hepfi.org
American Liver Foundation: www.liverfoundation.org
Hepatitis C Support Project: www.hcvadvocate.org
http://www.sacbee.com/content/news/story/14263918p-15076727c.html

Treatment works for drug addiction

2006-10-29 08:31:50

Treatment works for drug addiction
BY Dr STEVEN KW CHOW
THE United Nations estimates that there are about 185 million drug abusers
worldwide, of which about 15 million are heroin users.
Although smaller in numbers compared to other drug users, heroin users
contribute to the bulk of public health problems associated with drug addiction,
like the 40 million HIV infections worldwide. Heroin addiction is also
associated with a significant economic cost to governments - loss of productive
population, crime, medical care, and social welfare.
Statistics from the Agensi Anti-Dadah Kebangsaan (AADK) revealed that out of the
10,473 cases recorded from January to March 2005 in Malaysia this year, 46.2%
were new addicts and the remaining 53.8% were relapse cases.
The most frequently abused drugs were heroin (36%), morphine (30%), cannabis
(23%) and metamphetamine (7%)
The Malaysian government currently spends more than RM50mil a year for drug
rehabilitation alone.
However, current trends indicate that the number of drug users in the country,
currently registered at more than 270,000, could reach half a million by 2015,
which is the year that the government has vowed to make Malaysia drug-free.
Improving access and quality of care
There is an urgent need for a concerted nation-wide effort to improve access and
the quality of drug addiction treatment in the country. The message from us in
the treatment community to the public is that treatment works and that we need
to reduce the stigma associated with drug addiction, which hinders a great
number of addicts from seeking help.
For many years, the "treatment community", encompassing medical doctors,
substance abuse counsellors, psychologists, psychiatrists and social workers,
has maintained that drug addiction is a chronic disease. Studies have shown that
drug addiction shares many features with other chronic illnesses, including a
tendency to run in families (hereditary), and can in fact be treated quite
effectively using a holistic, medical approach. Effective medical treatment
addresses the multiple needs of the individual and not just drug use.
Opiate addiction in Malaysia
Up to very recently, heroin has been traditionally the main drug of abuse. The
official government statistics indicated 275,499 heroin addicts registered in
2004. WHO estimates that only one in four drug addicts are registered. Thus, the
extent of the problem that we may be facing is potentially mind-boggling. Heroin
addiction has a major impact on the cost of medical care in Malaysia as
exemplified by:
a.. Approximately 77% of all reported HIV cases are secondary to intraveneous
drug use (WPRO, 1999)
a.. High incidence of hepatitis C and pulmonary tuberculosis in drug addicts
a.. High cost of current programmes of compulsory drug rehabilitation with high
relapse rates.
Injecting drugs and needle sharing are major risk behaviours for HIV
transmission in drug users (Juita, 1995; Yoong, 1997), which accounts for an
estimated 12 to 56% of HIV infections in heroin users (Wang & Ismail, 1998; Lye
et al, 1994; Singh et al, 1993), except for sexual transmission, particularly
with cross-border unprotected sexual exposure in northern peninsular Malaysia.
Thus there is compelling evidence for instituting needle exchange and harm
reduction programmes in Malaysia. However it must be remembered that these
programmes deal only with one extreme of the spectrum i.e. the end-stage disease
scenario. It cannot and was never meant to be the model for a wholesome national
programme that should emphasise prevention and early treatment.
Treatment for heroin addiction
The face of opioid addiction treatment has been changing at a rapid pace with
the employment of various new strategies. Newer innovations, particularly
community-based treatment programmes, allow more people who are opioid-dependent
to have access to the treatment that they need.
In Malaysia, drug addiction has been treated with behaviour-based and
faith-based programmes. For some drugs, such as heroin, there is also treatment
with prescription medications. Treatment must however, go beyond just providing
a substitution medication. It must also include the development of job skills,
counselling and other ancillary services.
In Malaysia, two medications are currently registered for the substitution
treatment of heroin dependence, namely buprenorphine and methadone.
Methadone works by binding to opiate receptors in the brain to trigger a
substitution response (i.e. as an agonist). Buprenorphine on the other hand
works in two ways, firstly as a partial agonist and secondly by binding to the
receptor itself and actually blocking it from activation by agonists (ie. as an
antagonist). With its other action as a partial agonist, buprenorphine activates
the receptor but does not cause as much of a physiological change as does a full
agonist.
Buprenorphine was first marketed for the treatment of heroin dependence in
France in 1996, and subsequently followed by other countries. Today,
buprenorphine is registered and marketed in 37 countries worldwide, including in
all main reference countries (Australia, US, UK and most European countries and
in some Asian countries). Ever since its introduction, buprenorphine has been
widely accepted worldwide as an effective and a safe option in treating opiate
dependence for two reasons.
Firstly, buprenorphine, when used correctly, provides a wide safety margin with
significantly lower chances for severe overdose effects. It produces little
physical dependence or respiratory depression and produces only mild withdrawal
symptoms, even if withdrawn abruptly (Fudala et al, 1990; Jasinski Pevnick &
Griffith, 1978).
Secondly, buprenorphine's long duration of action allows for flexible,
patient-tailored dose administration. This wide safety margin makes
buprenorphine suitable for use in new treatment settings, such as an office
practice, as well as in the more institution-based traditional opioid treatment
programmes.
On the community level, treatment with buprenorphine has been shown to reduce
the harmful effects of opioid dependence by reducing drug use severity,
restoring productivity and social status of patients and decreasing the spread
of HIV/AIDS and other infectious diseases (Fhima et al, 2001; Kakko et al, 2003;
Mattick et al, 2003).
Methadone has been recently launched in Malaysia in a pilot treatment programme
at selected treatment centres. The earlier experience of methadone in Malaysia
in the early 70s had been disastrous due to widespread abuse of the medication
as a result of poor regulation and control.
The Buprenorphine experience in Malaysia - challenges to medical treatment
The potential for diversion and abuse of these prescription drugs has always
been a cause of concern for responsible members of the treatment community. The
treatment community's diligence and accountability in the dispensing of opioids
is absolutely crucial in maintaining the security of these treatment drugs and
to ensure that they are not abused by unscrupulous parties for mere profit.
Treatment clinics and office-based doctors are required to comply with
established federal regulations as well as recommended practice guidelines.
Additionally, good clinical governance requires the practitioner to institute
practices and procedures that will protect against inappropriate or illegal
prescribing of opioids.
Buprenorphine was introduced in November 2001 in Malaysia, and has been used
successfully for the past four years for detoxification and maintenance therapy.
On the positive side, the availability of this medication has enabled the hidden
heroin addicts to seek community-based treatment in their neighbourhood clinics
and to continue to live a productive life.
Despite the best of intentions, there have been reported cases of illicit
diversion of buprenorphine and injecting of prescribed buprenorphine. Based on
experiences in other countries, this undesirable activity is not unexpected in
the addict population. Invariably there will be a proportion (up to 25%) of
hardcore patients who will abuse their treatment regardless of what medication
is used.
To curb this problem, strict control measures were instituted in the supply and
distribution of buprenorphine. In the past, this has resulted in the disruption
of medication supply, which in turn destabilised the treatment environment for
patients who were in remission. Destabilisation of the treatment environment
provides the ideal environment for relapse and the failure of community-based
treatment.
In anticipation of this problem, the treatment community has pushed to put in
place an on-going integrated programme with the strategy of cultivating the
highest level of care in buprenorphine substitution treatment. This programme
aims to instil good clinical practice by the medical practitioners, improve
counselling skills, encourage family and community support and to educate the
public.
Newer medications that have additional safeguards against abuse are already in
the pipeline, like preparations combining buprenorphine and naloxone (an opiate
antagonist). Experiences in other countries have shown their superior efficacy
and safety in community-based treatment compared to currently available options.
In absolute terms, the number of addicts treated with buprenorphine (estimated
at 5,000) is very low compared to the total number of 275,499 registered heroin
addicts in Malaysia. There is currently a mismatch between the ability to
provide help and the amount of people needing help in community-based treatment.
Thus expanding the treatment community and maintaining a stable treatment
environment is of paramount importance for implementing a successful
community-based treatment programme.
a.. Dr Steven KW Chow is president of the Federation of Private Medical
Practitioners Associations Malaysia and founding chairman of DrsWhoCare. This
article is contributed by the Federation of Private Medical Practitioners
Associations Malaysia. For further information, e-mail
starhealth@.... The information provided is for educational and
communication purposes only and it should not be construed as personal medical
advice. Information published in this article is not intended to replace,
supplant or augment a consultation with a health professional regarding the
reader's own medical care. The Star does not give any warranty on accuracy,
completeness, functionality, usefulness or other assurances as to the content
appearing in this column. The Star disclaims all responsibility for any losses,
damage to property or personal injury suffered directly or indirectly from
reliance on such information.
http://thestar.com.my/health/story.asp?file=/2006/6/4/health/14430846&sec=health

Low Donors Means Diseased Organs Used

2006-10-29 04:46:20

Low Donors Means Diseased Organs Used
10:55 AM, 04 Jun 2006
A group promoting organ donation says the number being donated in New
Zealand is so low that doctors are having to use diseased organs.
Last year 29 people's organs were donated, and 18 had diseases including
hepatitis, diabetes and cancer.
The organ donor lobby group, Give Life New Zealand, says rules which
require family permission to be given before organs can be taken, need to
change.
The group's spokesman, Andy Tookey, says it is not surprising just under
half of all families decline a request to remove the dead person's organs.
Mr Tookey is asking people to support a member's bill before parliament
which would make an organ donor's wishes legally binding.
http://www.newswire.co.nz/main/viewstory.aspx?storyid=320157&catid=16

Traveling through the world of fake drugs (Chris Hansen, Dateline correspondent)

2006-10-28 15:46:39

If you didn't watch it tonight you missed a good show. I am sure they will have
it on again. Meanwhile, here are a couple of links that will tell you about
the scary possibility of getting counterfeit meds when you fill your RX's.
. June 2, 2006 | 11:10 a.m. ET
Traveling through the world of fake drugs (Chris Hansen, Dateline correspondent)
I have three basic rules for doing investigative reporting in countries where
governments frown on this sort of activity: get in quietly, get out quickly and
make sure the video tapes make it back to New York.
In the case of our investigation into the world of counterfeit medicine we were
fortunately able to accomplish all three. We had heard from people in federal
law enforcement and major drug companies that the production of counterfeit
medicine is exploding in places like China, Pakistan and India just to name a
few.
About a year ago, we decided to try to turn our hidden cameras on this subject
and now we're going to take you along as we see first hand how counterfeit
medicines can be smuggled into the U.S. without detection and perhaps even more
alarming, how they could end up in your neighborhood pharmacy.
We posed as a company called The Hansen Group and started trolling the Internet
looking for suppliers of counterfeit medicines. Within weeks, companies all over
the world began offering us everything from fake Viagra to knock off Tamiflu,
the drug that would be the first line of defense during a bird-flu pandemic. The
supply line took us all the way to Hong Kong, where in a modern hotel room
outfitted with hidden cameras, we met with a woman who told us she was a major
player in this illicit business. Even we were surprised when the woman, who
called herself Cherry Wong, agreed to ship us thousands of fake Viagra tablets a
week, a deal that could be worth $10 million.
Pfizer, which makes Viagra tested some of Cherry's product and found it to be,
in fact, counterfeit, although it did contain some active ingredient.
It is an eye-opening investigation and personally alarming to see how much
counterfeiting is going on. These drugs can obviously be very dangerous on many
different levels.
And while you might think that by avoiding buying medicine over the Internet you
can protect yourself, think again. As you'll see in our story, medicine doesn't
usually go straight from the factory to the pharmacy. There is a complex network
of wholesalers who buy and sell surplus drugs. In some cases, all it takes is
some phony paper work and some realistic packaging for fake medicine to slip
into the system.
The report on counterfeit drugs airs Sunday, 7 p.m. June 4, on Dateline NBC.
Click here for more info, resources on fake drugs.
http://www.msnbc.msn.com/id/13099555/
http://www.msnbc.msn.com/id/3032600/

Re: [HepCingles2] Are You Growing Up, Or Just Growing Older?

2006-10-28 15:22:42

Hi scalihepc,
Thank you for sharing this.
Is there more material on this subject?
It is straight forward and easy to understand.
This issue has been on my mind alot lately, and I think I'm slowly
changing,but that may be because it's some sort of "natural process," but I
still need a map and haven't found one yet.
Maybe it's because the brain/body are finally cleared from Alcohol/Drugs
(after 2 1/2 yrs cleanand 30+ yrs. of using )..If I understand correctly, is
emotional immaturity mostly caused by low self esteem, or staying loaded and
avoid dealing with life/relationship/job
issues? or both?
Help in Houston,
Del

Fed: Many drug agencies failing to test users for hepatitis

2006-10-28 03:02:29

Fed: Many drug agencies failing to test users for hepatitis
Australian Associated Press - Jun. 04, 2006
SYDNEY, June 4 AAP - A significant number of injecting drug users are not being
tested for hepatitis and other blood-borne diseases despite national public
health policies, a survey has found.
Transmission of blood-borne viruses among drug users is still a considerable
problem in Australia, with hepatitis B and C still spreading rapidly.
A survey of 222 drug and alcohol services has found that while about 75 per cent
offer some testing and vaccinations for these conditions and HIV, fewer then
half do so routinely.
The study, published today in the Medical Journal of Australia, also found only
one third offer these services routinely onsite.
The authors said the results were at odds with testing policies repeatedly
issued by national health organisations.
They were particularly disappointing given the National Health and Medical
Council's call more than 20 years ago for across the board vaccinations for
hepatitis B.
"That a sizeable proportion of drug and alcohol agencies do not provide
cost-effective, evidence-based (blood-borne disease) interventions to this
marginalised and high-risk group is inconsistent with Australian policy," they
wrote.
It was also out of step with the "expectation of reasonable public health care
and harm reduction".
The researchers, from Sydney South West Area Health Service and Auckland
University, said the lack of services left many users without an understanding
of their conditions.
The delays in detection meant delays in specialist referrals and the lifestyle
changes needed to slow the disease's progression.
The authors called for more funding for onsite testing and vaccinations "so
testing becomes part of the core business for more drug treatment agencies".
They also suggested adopting more rapid vaccination schedules and better
co-ordination between health services.
Previous surveys indicate that between 50 and 60 per cent of users have
hepatitis C and between 23 and 52 per cent have hepatitis C.
Only between one and three per cent have HIV - a figure which has remained
consistently low since sterile needle programs were introduced in the 1980s.
http://www.therapeuticsdaily.com/news/article.cfm?contentValue=940068&contentTyp\
e=sentryarticle&channelID=31

Re: Are You Growing Up, Or Just Growing Older?

2006-10-27 21:40:53

Dell,
I'm always reading things like this, if you want I can share them
with you as I find them. Addictions to drugs and alcohol leave people
emotionally immature. There is no emotional growth at all while
addicted, it stops when the addiction starts. I found all that out
the hard way. I still have certain things I'm working on, but at
least I do. I've known a lot of people who quit all the addictions
but keep the same lifestyle patterns. Many of them never mature
emotionally. It's nice to know that there are others out there who
care enough about themselves enough to work on it. Good for you.
Vickie

Efforts focus on fighting hepatitis in Georgia

2006-10-27 15:46:51

Efforts focus on fighting hepatitis in Georgia
By PATRICIA GUTHRIE
The Atlanta Journal-Constitution
Published on: 02/12/06
Saving more Georgians from the ravages of hepatitis will be the focus of
exhibits and and a press conference Monday at the Capitol.
Several organizations, physicians and patients, say they plan to lobby for more
funding for hepatitis screening and prevention.
Hepatitis is a viral disease that inflames the liver, and can lead to cirrhosis,
liver cancer, liver failure and early death. Three different viruses cause the
three forms of hepatitis, known as A, B, and C.
"Hepatitis is the pandemic that no one is talking about," said Fred Thompson,
CEO of the American Liver Foundation, one of several national experts expected
today. "Many people are infected and then they unwittingly spread it."
Georgia's rates of hepatitis are two to three times the national average.
Contributing factors include a large population of people living with HIV/AIDS,
immigrants moving from hepatitis-plagued countries, and little prevention in
Georgia prisons, health officials say.
Hepatitis A is typically spread through contaminated food and water; hepatitis B
is spread through sex or contaminated blood, hepatitis C , the most deadly of
the three, is transmitted through sex, dirty needles or contaminated blood.
Infants can also be infected by their mothers.
Medical and social costs of the disease are expected to soar in coming years as
infected people begin experiencing debilitating symptoms.
About 260 Georgians need liver transplants; most of them suffer advanced
hepatitis
People can get vaccinated for hepatitis A and B. But hepatitis C has no vaccine
and no cure. It's an insidious infection that can attack the body for 20 years
or more before symptoms lead to a diagnosis. By that time, liver damage is
irreversible.
Most physicians don't routinely test for hepatitis, and most people don't know
why the blood test is important, said Cathalene Teahan, a nurse and lobbyist for
the Georgia AIDS Coalition.
Most county health clinics in the state also don't offer Hepatitis C screening,
she said.
The group plans to request money for routine hepatitis B vaccinations in Georgia
prisons because studies show that prisoners commonly spread the disease upon
being released.
http://www.ajc.com/search/content/metro/stories/0213metleghepatitis.html

Chat reminder!, 2/15/2006, 9:30 pm

2006-10-27 13:44:07

Reminder Reminder from the Calendar of HepCingles2
Chat reminder!
Wednesday February 15, 2006
9:30 pm - 1:30 am
This event repeats every week.
The next reminder for this event will be sent in 18 hours, 4 minutes.
Event Location: Chat Room at HepCingles2

Fwd: For those who have children and grandchildren . . .

2006-10-27 07:36:45

Hi everyone.
This IS an eyeopener.
I don't have kids but I had no idea there were this many sick demented people
out there. there about 8 within walking distance of me.
If you don't want to know if you are living near a sex offender, delete this
now.
If you do...just click on the site.
I forward this with the intention of doing good...if someone gets upset, You
should have deleted it.
Del
Note: forwarded message attached.

like it;

2006-10-27 02:06:07

Hello group and happy belated St.Valentine's Day! Say Alfie, I have'nt
been posting on a steady basis but always read some of this group's
writing.Alfie-I LIKE your writing and will always read your material.
Given the situations, meds., and emotional ups and downs, some
latitude should be a given "anyway"! And I don't find anything
juvenile so far. Would like it if you would write directly to my e-
mail sometimes. Thankyou, AL., alfottos@...

Anti-D for Treating Thrombocytopenia in Adults Infected With Hepatitis C Virus With or Without HIV Co-Infection

2006-10-26 20:44:36

Anti-D for Treating Thrombocytopenia in Adults Infected With Hepatitis C Virus
With or Without HIV Co-Infection
This study is currently recruiting patients.
Verified by National Institute of Allergy and Infectious Diseases (NIAID)
December 2005
Sponsored by: National Institute of Allergy and Infectious Diseases
(NIAID)
Information provided by: National Institute of Allergy and
Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier: NCT00239733
Purpose
Thrombocytopenia occurs when a person's blood has a decreased number of
platelets, which are cells involved in blood clotting. This condition may lead
to uncontrolled bleeding and can be fatal. Thrombocytopenia commonly occurs with
hepatitis C virus (HCV) infection or as a result of standard HCV treatment.
Anti-D is an antibody approved by the Food and Drug Administration (FDA) for the
treatment of HIV-related thrombocytopenia. The purpose of this study is to
determine the safety and effectiveness of intravenous anti-D for the treatment
of thrombocytopenia in patients with HCV infection who are starting or already
undergoing treatment with peginterferon alfa-2 and ribavirin. This study will
recruit HCV patients both with and without HIV co-infection.
Condition Intervention
Thrombocytopenia
Hepatitis C
HIV Infections
Drug: Anti-D
MedlinePlus related topics: AIDS; Bleeding Disorders; Hepatitis C
Genetics Home Reference related topics: Bleeding Disorders
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group
Assignment, Safety/Efficacy Study
Official Title: The Safety and Efficacy of Intravenous Anti-D for the Treatment
of Thrombocytopenia in Patients With HCV Infection Prior to or During Treatment
With Pegylated-Interferon and Ribavirin
Further study details as provided by National Institute of Allergy and
Infectious Diseases (NIAID):
Primary Outcomes: Frequency and severity of adverse events; Absolute change in
platelet count from baseline to Weeks 1, 4, and 12 after initiating treatment
Expected Total Enrollment: 20
Study start: March 2005
Peginterferon alfa-2 with ribavirin is the current standard of care for the
treatment of HCV infection; however, severe hematologic effects, including
anemia, leukopenia, and thrombocytopenia, may make this treatment less than
ideal for patients with HCV. Medications to prevent or treat serious neutropenia
and anemia have been established and are commonly used. However,
thrombocytopenia remains a barrier to the effective treatment of HCV infection
in some patients. Developing a more effective treatment for thrombocytopenia for
these patients would decrease the risk of serious bleeding events. It may also
improve HCV treatment outcomes by preventing dose modifications or
discontinuations of peginterferon alfa-2 and ribavirin due to thrombocytopenia.
Anti-D is an antibody to the Rh (D) antigen on red blood cells. When anti-D
attaches to the Rh (D) antigen, immune-mediated destruction of platelets is
prevented, helping to alleviate low platelet levels in people with
thrombocytopenia. This study will investigate the safety and efficacy of anti-D
for the treatment of thrombocytopenia in HCV patients currently on or starting
standard HCV treatment. Both HIV infected and uninfected participants will be
recruited for this study.
This study will last 12 weeks. Participants in this study must be either
currently on peginterferon alfa-2 and ribavirin treatment or initiating such
treatment at the start of the study; these two medications will not be provided
by the study. At study entry, participants will be given anti-D over a 30-minute
infusion in an outpatient setting. Participants will be observed for any adverse
effects for 1 hour postinfusion. Some participants may require additional doses
of anti-D later in the study, depending on individual response to the drug;
participants may receive 1 to 6 doses of anti-D. Efficacy of anti-D treatment
will be assessed by absolute change in platelet count and the ability to sustain
plaletet counts greater than 50,000 cells/microL during the study. Cytokine
levels will also be monitored to gain insight on how anti-D may work with
cytokines in platelet survival and clearance.
Generally, study visits will occur at study entry and Weeks 1, 2, 4, 8, and 12.
In patients who require additional infusions of anti-D, there will be additional
visits scheduled for each additional infusion and a postinfusion visit occurring
1 week after each infusion. All study visits will include medication history and
blood collection. A clinical assessment and a targeted physical exam will occur
at study entry, Weeks 1 and 12, and at additional infusion and postinfusion
visits, if applicable.
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria for All Participants:
a.. HCV infected
b.. Currently on treatment for HCV OR plan to begin treatment for HCV at the
start of this study
c.. Platelet count less than 50,000 cells/microl
d.. Hemoglobin greater than 10 g/dl OR greater than 11 g/dl if peginterferon
treatment-naive
e.. Red blood cells are Rh (D) antigen-positive
f.. Negative Coombs direct antibody test
Inclusion Criteria for HIV Infected Group:
a.. HIV infected
Inclusion Criteria for HIV Uninfected Group:
a.. HIV uninfected
Exclusion Criteria:
a.. Prior treatment with intravenous immunoglobulin (IVIG), anti-D, or other
medication for the treatment of thrombocytopenia within 30 days of study entry
b.. Prior serious reaction to plasma products
c.. Absence of spleen
d.. Evidence of thrombotic thrombocytopenic purpura (TTP) OR cause of
thrombocytopenia other than HCV infection, HCV treatment, or HIV infection
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00239733
Kristen M. Marks, MD 212-746-7187 markskr@...
New York
New York Presbyterian Hospital (Cornell), New York, New York, 10021,
United States; Recruiting
Kristen M. Marks, MD 212-746-7187 markskr@...
Kristen M. Marks, MD, Principal Investigator
James Bussel, MD, Sub-Investigator
Andrew Talal, MD, MPH, Sub-Investigator
Marshall Glesby, MD, PhD, Sub-Investigator
Roy (Trip) Gulick, MD, MPH, Sub-Investigator
Study chairs or principal investigators
Kristen M. Marks, MD, Principal Investigator, Weill Medical College of Cornell
University
More Information
Click here for more information about peginterferon alfa-2
Click here for more information about ribavirin
Publications
Ware RE, Zimmerman SA. Anti-D: mechanisms of action. Semin Hematol. 1998
Jan;35(1 Suppl 1):14-22. Review.
Study ID Numbers: K23AI65319-01; K23AI65319-01
Last Updated: December 6, 2005
Record first received: October 13, 2005
ClinicalTrials.gov Identifier: NCT00239733
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2006-04-03
http://www.clinicaltrials.gov/ct/show/NCT00239733

scary but useful..thx Del

2006-10-26 12:12:42

THIS IS TRULY SCARY........ BUT POSSIBLY VERY USEFUL.
Know who your neighbors are
Okay, here's the deal... enter your address... it
will show a "house", that's yours... all the little colored boxes are
Sex Offenders... click on them and you get a name & picture of the
person along with his crime... pretty amazing and scary...
Pass this on to your friends and family.
http://www12.familywatchdog.us/!
~Bayla~
One who knows how to show and to accept kindness
will be a friend better
than any possession.
-Sophocles

A letter to the victims of hepatitis C

2006-10-26 08:01:35

This morning I woke, and I heard someone spoke, of the promises
given to revoke; this incidious disease, which we need not appease,
its silent in its actions, but comes on like a stealth bomber, and
we wonder.?
We live a life of many days of distraught; wondering if our memories
are going to stay in the forefront.?
We need to find a real cure to this disease, as it is playing with
our minds, and let me tell ya its not a tease.
I make no excuses for my cognitive thought disorder, just know that
this is part of the virus I have not overcome; but with this disease
I will fight till the end, because its the only way to learn how to
win?
If your not a sufferer of this disease we call the dragon, but are
aflicted by the patterns of our misbeavin', please understand we are
giving it our best , but we need the medical world to bring to the
forefront the cure.
Iam alone because I believe this disease spent many years effecting
my thinking.
I choose this life to be alone, but I struggle with the lonliness
and sometimes hate to come home, so please understand we didn't just
cop out" altho now Iam dating and getting out;)
Read the information thats out there, that spells it out.
You do have time don't you when your trying to find out; what makes
us so crazy or unstable in our lives, or vulnerable, and too
sensitive and we tend to just cry?
Being too sensitive; well I wonder why we are? We have a virus
running through every part of our minds and livers, and blood as
well, wouldnt you be a bit sensitive, even if you didnt know?
Take time to tell a loved one today you love them as you did before
this dismay. We need to know we are loved as are you, to understand
our disease isnt hard to do.
Comparitively to AIDS or Cancer; many hoover over the patient in
wonder? sadness hits them;the friends,family and all, but because
our disease hcv is so silent you just watch us try to walk tall.
But many of us are worn frazzled and torn, please dont judge the
recipient till you have lived in our shoes, as we are the people
whom have been labeled in this world ; as the ones whom brought this
on, ourselves with our drug living world. Nope not going to buy
that,what a facade; tainted blood is a big mode of contraction that
we had no idea; so please don't judge us, go to the source, be
affirmative and proactive and fight for the Cure, without you non
heppers we will go out in this world.
No rememberences of hero's; heck we dont need that big a movie; but
we would ask that you'd spend some time telling the facts, educating
and advocating and getting the real "truths" out of our
contraction , do it for us will you? As we are worn and tired and
because of the way this disease effects our minds, and to take a
pill won't bring us back to who we were, but your kindness and love,
and steadfastness to visit us, thats what we need , we are at a loss.
We have no promises each day we get up; but I have every symptom of
this illness without a doubt, Iam not able to treat with interferon
based drugs, but I can just sit and wait, till Iam lifted above.
Please understand our cry; its very public and clear; we need your
dearness and understanding not judgements or just sneer, for you see
we live a life you will never understand; its called the life of a
silent virus, going through our homeland.
Iam at a loss of words for how do you feel? when asked? as I act as
if? huh; I'am tired of that.!!! We are people with feelings like the
AIDS vicitims, why do you leave us in the background and tend to
withdraw? are you uncomfortable with the person you see, only look
in the mirror, at the one you could be, a silent advocate whom cares
about the world, one that isnt caught up in the toys, or your own
fun times, take us with you someday give it a try , you might find
out how much more self fulfilling it is to try.!!
Its time to break this code of silence in our homeland, and turn it
around, give us a helping hand. If you turn away thats ok, but we
know whom cares and who's too busy wanting to play.? We need you
healthy people to come with us to the Hill , and fight for the
rights of Hepatitis C and its drill.!!!!!!!!! ~author unknown~

Interim Results of Studies of Albuferon plus Ribavirin in Nonresponders and in Treatment-naïve Patients with HCV Genotype 1

2006-10-26 04:59:03

Interim Results of Studies of Albuferon plus Ribavirin in Nonresponders and in
Treatment-naïve Patients with HCV Genotype 1
Human Genome Sciences (HGS) this week reported interim results of two clinical
trials to evaluate the safety, tolerability and efficacy of the experimental
drug Albuferon (albumin-interferon alfa-2b) in combination with ribavirin for
the treatment of chronic hepatitis C. One study evaluates the drug's activity in
nonresponders to previous treatment with conventional interferon alfa therapy
and the other in individuals without any prior therapy.
A product of albumin fusion technology used to improve the pharmacological
properties of interferon alfa, Albuferon is a novel, long-acting form of
interferon alfa.
Interim results of the Phase 2 clinical trial in nonresponders demonstrate that
Albuferon in combination with ribavirin is safe, well tolerated and "shows
robust antiviral activity," according to the company's announcement. A
presentation of the full interim data will take place on April 30 at the
European Association for the Study of the Liver (EASL) in Vienna, Austria, April
26-30, 2006 [1].
In a separate press release issued today, HGS announced the interim results of a
larger Phase 2b clinical trial of Albuferon in combination with ribavirin versus
Pegasys plus ribavirin in treatment-naïve patients with chronic hepatitis C
genotype 1 [2]. Following is the text of the announcement by HGS on the Phase 2
and Phase 2b studies:
David C. Stump, MD, Executive Vice President, Drug Development, said, "I
continue to be encouraged by the growing evidence that Albuferon in combination
with ribavirin is safe and well tolerated, with robust and durable antiviral
activity. The results available from the first three treatment groups for the
48-week treatment period of the Phase 2 study demonstrate that Albuferon was
well tolerated at all doses administered, with no significant increase in
severity of adverse events between Week 12, Week 24 and Week 48.
Decreases in hematologic cell counts were well managed with dose reductions, and
returned to baseline following the completion of therapy. I am also encouraged
by the emerging evidence of clinically significant antiviral effect.
At Week 48, 30% of the patients in the three lower-dose treatment groups had no
detectable hepatitis C RNA viral load. At the 12-week follow-up point, 18% of
the patients continued to have no detectable hepatitis C RNA viral load.
These data are quite positive, considering that they were observed in a heavily
pretreated population, nearly two thirds of whom previously failed to respond to
treatment regimens that included pegylated interferon alfa-2a (Pegasys) plus
ribavirin.
The results to date also indicate that both the 1500-mcg and the 1800-mcg doses
were well tolerated, with safety data generally similar to the lower-dose
treatment groups and with greater antiviral activity.
Results at the higher doses in the current Phase 2 study encourage us to
evaluate a regimen in interferon-naïve patients that combines higher doses of
Albuferon with ribavirin administered at intervals of 28 days. We look forward
to the complete presentation of these interim data at the EASL meeting in April,
and to continuing the evaluation of Albuferon in combination with ribavirin at
higher doses and over the full term of the current study."
The Phase 2 trial is a randomized, open-label, multi-center, dose-escalation
study, and is being conducted in the United States. The study design states that
approximately 50 percent of the subjects enrolled should be patients who have
failed combination therapy that included pegylated interferon alfa plus
ribavirin.
A total of 115 patients have been enrolled into 5 Albuferon treatment groups
that are receiving doses of Albuferon ranging from 900-1800 mcg [1, 3-5].
Patients were initially randomized into 3 Albuferon treatment groups (900 mcg at
14-day intervals, 1200 mcg at 14-day intervals, and 1200 mcg at 28-day
intervals).
Following evaluation of safety data, 2 additional cohorts were enrolled
sequentially (1500 mcg at 14-day intervals and 1800 mcg at 14-day intervals).
Patients are receiving Albuferon administered subcutaneously, with all patients
receiving weight-based oral ribavirin daily at 1000 or 1200 mg in two divided
doses. Patients in the trial will receive 48 weeks of treatment, with an
additional 24 weeks of follow-up.
The primary objective of the Phase 2 study is to evaluate the safety and
tolerability of Albuferon in combination with ribavirin. The study also is
evaluating the efficacy of Albuferon in combination with ribavirin. The primary
efficacy endpoint is sustained virologic response (SVR), defined as undetectable
virus 24 weeks after the end of therapy.
Data are available through Week 48 (end of treatment) on 71 patients who were
enrolled in parallel and randomized into three Albuferon treatment groups:
900 mcg administered subcutaneously every 14 days;
1200 mcg administered subcutaneously every 14 days; and
1200 mcg administered subcutaneously every 28 days.
All patients are receiving weight-based oral ribavirin daily at 1000 or 1200 mg
in two divided doses. Of the subjects in the first three Albuferon treatment
groups, 65% (46/71) were non-responders to pegylated interferon alfa, and 93%
(66/71) were infected with genotype 1 hepatitis C.
More than 60% of the study subjects had received more than one prior interferon
alfa-based treatment regimen, and the mean duration of prior therapy was
approximately 15 months.
At Week 48, 30% (21/71) of the patients exhibited no detectable HCV RNA viral
load. Antiviral activity was similar for the 14-day and 28-day Albuferon
treatment groups. At the Week 12 follow-up after the end of treatment, 18%
(13/71) of these heavily pretreated patients had no detectable hepatitis C RNA
viral load.
Albuferon in combination with ribavirin was well tolerated. The incidence of
adverse events was similar across the three dose groups for which 48-week data
are available, and generally similar to the adverse events observed in the 2
higher-dose groups (24-Week data for the 1800-mcg and 1500-mcg cohorts).
There was no increase in severity of adverse events beyond Week 12. Hematologic
reductions were maximal by Week 8, were well managed with dose reductions, and
returned to baseline following the completion of therapy (Week 12 follow-up
after the end of 48 weeks of treatment).
Albuferon appeared to be better tolerated in the treatment group receiving 1200
mcg administered subcutaneously every 28 days, with fewer hematologic dose
reductions observed in this group. No subject required discontinuation of either
Albuferon or ribavirin for hematological abnormalities.
Overall, the rate of treatment-emergent Albuferon antibodies is 10%, with
pre-existing antibodies detected in 17% of study participants. There was no
apparent correlation between the emergence of antibodies and antiviral response,
adverse events or pharmacokinetics. No overall increase in the emergence of
antibodies was observed between Week 12, Week 24 and Week 48, or in
administration of higher doses.
Data are available through Week 24 for treatment groups receiving, in
combination with ribavirin, Albuferon doses of 1500 mcg and 1800 mcg,
respectively, administered subcutaneously every 14 days.
At Week 24, the same percentage of patients in the 1500-mcg and 1800-mcg
Albuferon treatment groups exhibited no detectable hepatitis C RNA viral load:
32% (7/22) in each of the two groups.
Data also are available for the 1500-mcg and 1800-mcg Albuferon treatment groups
on early virologic response (EVR12). EVR12 is defined as a
greater) reduction in HCV RNA viral load at Week 12. In the 1500-mcg treatment
group, 41% or the patients (9/22) achieved EVR12. In the 1800-mcg treatment
group, 59% (13/22) of the patients achieved EVR12.
The 1800-mcg Albuferon treatment group had a higher percentage of genotype 1
hepatitis C patients who had failed to respond to previous treatment with a
combination of pegylated interferon and ribavirin - 91% (20/22) versus an
average of 66% (61/93) in the other Albuferon treatment groups combined.
At Week 24 in this important and most difficult to treat subgroup, the data show
the following percentages of patients with no detectable HCV RNA viral load: 17%
(2/12) in the treatment group receiving 900 mcg of Albuferon at 14-day
intervals; 19% (3/16) in the treatment group receiving 1200 mcg of Albuferon at
14-day intervals; 15% (2/13) receiving 1200 mcg of Albuferon at 28-day
intervals; 27% (4/15) receiving 1500 mcg of Albuferon at 14-day intervals; and
32% (6/19) receiving 1800 mcg of Albuferon at 14-day intervals.
Data also are available for this subgroup on early virologic response (EVR12).
The data show the following percentages of patients achieving EVR12:
42% (5/12) in the treatment group receiving 900 mcg of Albuferon at 14-day
intervals;
25% (4/16) receiving 1200 mcg of Albuferon at 14-day intervals;
23% (3/13) in the treatment group receiving 1200 mcg of Albuferon at 28-day
intervals;
33% (5/15) receiving 1500 mcg of Albuferon at 14-day intervals; and
63% (12/19) receiving 1800 mcg of Albuferon at 14-day intervals.
Safety data available for the 1500-mcg and 1800-mcg treatment groups through
Week 24 are generally similar to the lower-dose Albuferon treatment groups. No
increase in the emergence of Albuferon antibodies was observed related to
administration of the higher doses.
Wall Street Reaction to Albuferon Results
Shares of Human Genome Sciences (HGS) fell 20 percent on March 14 after interim
study results of Albuferon plus ribavirin drew mixed reactions from Wall Street,
according to an article in the Washington Post.
HGS said in a conference call with analysts that two Phase 2 human studies
showed encouraging results and support the continued development of the drug for
chronic hepatitis C. But the study results left some investors uncertain how
well the drug, even if it wins approval from the Food and Drug Administration
(FDA), will be able to compete with established treatments that have been on the
market for years, i.e. peginterferon alfa-2a (Pegasys) and peginterferon alfa-2b
(PegIntron).
Standard & Poor's, widely respected on Wall Street for the impartiality of its
research, upgraded the HGS shares to "buy" from "hold." But Infinium Capital
Corp. maintained a negative rating on the stock.
03/17/06
Sources
Human Genome Sciences
J Gillis. Investors Unhappy With HGS Drug Test Data. Washington Post. Page D01.
March 15, 2006.
References
1. V Rustgi and others. A Phase 2 dose-escalation study of Albuferon combined
with ribavirin in non-responders to prior interferon based therapy for chronic
hepatitis C infection. 41st Annual Meeting of the European Association for the
Study of the Liver (EASL), Vienna . Oral Presentation #113.
2. (HGSI Press Release) Human Genome Sciences Announces Positive Interim Results
of Phase 2b Clinical Trial of Albuferon in Combination with Ribavirin in
Treatment-Naïve Patients with Chronic Hepatitis C. March 14, 2006.
3. D R Nelson and others. A Phase 2 study of Albuferon in combination with
ribavirin in non-responders to prior interferon therapy for chronic hepatitis C.
56th Annual Meeting of the American Association for the Study of Liver Diseases
(AASLD), 2005. Oral Presentation #204.
4. (HGSI Press Release) Human Genome Sciences Reports Interim Results of Phase 2
Clinical Trial of Albuferon in Combination with Ribavirin in
Treatment-Experienced Hepatitis C Patients. November 15, 2005.
5. It is important to note that the method of measurement for dose determination
in the Phase 2 study of Albuferon in combination with ribavirin in
treatment-experienced patients (as well as in other Phase 2 studies of the
compound) is different from the method of measurement in the Phase 1/2 study of
Albuferon. Accordingly, the 900-mcg dose in the current study is equivalent to a
680-mcg dose in the Phase 1/2 study, and the 1200-mcg dose is equivalent to 900
mcg in the Phase 1/2 study.
http://www.hivandhepatitis.com/hep_c/news/2006/031706_a.html

RE: [HepCingles2] scary but useful..thx Del

2006-10-25 12:30:29

Hey all....copy and paste the URL below, and then delete the ! before
hitting 'enter', otherwise the page won't come up. Interesting stuff...and
scary! I wonder how current the information is.
**hugs**
Alfie

Hep C Treatment help.

2006-10-25 11:27:03

Hey Guys, I am new here so hello all.
I have Hep C, have for about 8 years and when I was diagnosed my DR
wanted to wait awhile befor we thought about interferon treatment.
Saying the drug at the time wasnt worth it. He was also concerned
about the side effects and at the time I was a year off of a 8 year
heroin addiction. I know am going on 8 years off all drugs and booze
so he now wants to start the treatment and he says the drug has come
a long way now.
So I started looking around about this interferon treatment and it
seems to me that this drug hasnt come along way at all. I was
reading all kinds of horror stories and lawsuits about treatment.
Espicially this company Schering-Plough; people are calling them
devils and poison makers. Are the only people who make interferon
that Hep C patients take? Are there safer/other brands of interferon
to take and also which brands should I never take?
The way I see things is I know Hep C can haunt me in the long run
but I start this treatment and end up with bad memory and am
depressed or even worse with brain damage or something else that is
terrible for the rest of my life...Well I would rather live out what
I got left with my faculties as they are now.
So any help in this worry of mine would be great. I do know this
treatment is different for all who take it but are the majority of
the ones that do ending up with worse condtions and other ailments
after the treatment.
Thanks,
Michael.

Rise in drug users getting HIV

2006-10-25 11:25:50

Rise in drug users getting HIV
17/03/2006 16:46 - (SA)
London - The number of injecting drug users infected with HIV in England and
Wales reached a 13-year peak in 2005, as the rate of infection rose sharply
outside London, the government said on Friday.
The Health Protection Agency said 1.6% of injecting users were infected, up from
0.9% in 2002.
"This is the highest level of infection since 1992, when one in 62 (1.6%)
injecting drug users were infected with HIV," the agency said on its Web site.
The number of infected drug users remained steady in London, but increased in
other cities from 0.2% in 2002 to 1.2% in 2005.
The agency said the number of HIV diagnoses among injecting drug users in 2005
could reach 182, up from 131 the year before.
The report "coincides with a reported increase in more risky behaviours among
injecting drug users, as well as a rise in hepatitis C infection," said Peter
Borriello, director of the Health Protection Agency's Centre for Infections
Diseases..
He said there was evidence of a rise in the injecting of crack cocaine, which
may be linked to the transmission of viruses like HIV and hepatitis C.
http://www.news24.com/News24/World/News/0,,2-10-1462_1900218,00.html

Human Genome Sciences Announces Positive Interim Results of Phase 2b Clinical Trial Of Albuferon(TM)

2006-10-24 20:01:00

Human Genome Sciences Announces Positive Interim Results of Phase 2b Clinical
Trial Of Albuferon(TM) in Combination With Ribavirin in Treatment-Naive Patients
With Chronic Hepatitis C
- Interim 12-Week Data Suggest At Least Comparable Antiviral Activity Versus
Pegasys, With Less Frequent Dosing -
ROCKVILLE, Md., March 14 /PRNewswire-FirstCall/ -- Human Genome Sciences, Inc.
(NASDAQ: HGSI) today announced 12-week interim data from a Phase 2b clinical
trial to evaluate the efficacy and safety of Albuferon(TM) (albumin-interferon
alpha 2b) in combination with ribavirin in patients with genotype 1 chronic
hepatitis C who are naive to interferon alpha-based treatment regimens.(1) The
results to date demonstrate that Albuferon in combination with ribavirin was
safe, well tolerated and showed robust antiviral activity. A presentation of the
full interim data will take place on April 29 at the European Association for
the Study of the Liver (EASL).(2)
In a separate press release issued today, HGS reported the interim results of a
Phase 2 clinical trial of Albuferon in combination with ribavirin in
treatment-experienced patients with chronic hepatitis C.(3-4)
David C. Stump, M.D., Executive Vice President, Drug Development, said, "The
interim results available to date from our Phase 2b trial are encouraging and
supportive of our broadening program of clinical study of Albuferon.(1-12) We
believe that an interferon with less frequent dosing than pegylated interferon,
and with comparable safety and efficacy, would be an important therapeutic
option for patients with chronic hepatitis C. Based on the 12-week virologic
response data from the Phase 2b study, Albuferon appears capable of meeting this
target at doses of 900-1200 mcg every 14 days. We are encouraged that the
interim data at the 1200-mcg dose administered every two weeks show a trend for
greater antiviral activity for Albuferon, compared with Pegasys administered
every 7 days, with 75% of the patients in this group exhibiting a level of
hepatitis C viral load below the level of quantitation, compared with 66% in the
treatment group receiving 180 mcg of Pegasys at 7-day intervals. Response rates
were somewhat lower at 12 weeks for the treatment group receiving 1200-mcg doses
of Albuferon every 28 days, which suggests that higher doses will be required to
optimize a 28-day dosing schedule. In other Phase 2 studies, we are evaluating
Albuferon doses of 1500 mcg and 1800 mcg. Interim results show that these doses
are well tolerated when given every 14 days and may have greater antiviral
activity than the 900-mcg and 1200-mcg doses on the same schedule.(3-4)
"The 12-week data from the Phase 2b trial show that Albuferon in combination
with ribavirin was well tolerated at all doses studied, with no discontinuations
due to hematological abnormalities. The fewest dose reductions due to drops in
hematologic cell counts were observed in the treatment group receiving 1200 mcg
at 28-day intervals. These data support the continuing exploration of a
treatment regimen that administers Albuferon at 28-day intervals with higher
exposures than those investigated in the current trial. We look forward to
presentation of the complete Phase 2b 12-week interim data set at the EASL
meeting in April, and to continuing the evaluation of Albuferon in combination
with ribavirin at higher doses and over the full term of the current study.
Assuming that positive data continue to emerge from this Phase 2b study and our
other ongoing Phase 2 trials of Albuferon, we plan to meet with clinical experts
and regulatory authorities to discuss the initiation of Phase 3 development of
Albuferon by year-end 2006."
The Phase 2b trial is a randomized, open-label, multi-center, active-controlled,
dose-ranging study being conducted in Australia, Canada, Czech Republic, France,
Germany, Israel, Poland and Romania.(1) A total of 458 patients with chronic
hepatitis C genotype 1 have been enrolled and randomized into four treatment
groups, three of which receive subcutaneously administered Albuferon (900 mcg at
14-day intervals, 1200 mcg at 14-day intervals, and 1200 mcg at 28-day
intervals(13)). The fourth treatment group serves as the active control group
and receives 180-mcg doses of subcutaneously administered peginterferon alfa-2a
(Pegasys) at 7-day intervals. All patients receive weight-based oral daily
ribavirin at 1000 or 1200 mg in two divided doses. The primary objectives of the
Phase 2b study are to evaluate the efficacy and safety of Albuferon in
combination with ribavirin, vs. Pegasys with ribavirin, in interferon
alpha-naive patients with chronic hepatitis C genotype 1. The primary efficacy
endpoint is sustained virologic response (SVR), defined as undetectable virus 24
weeks after completion of 48 weeks of treatment.
Virologic response and laboratory data are available on 458 patients through
Week 12 of the Phase 2b trial. The data show the following percentages of
patients with hepatitis C (HCV) RNA viral load below the level of quantitation
(43 IU/mL) at Week 12: 66% (75/114) in the treatment group receiving 180-mcg
doses of Pegasys at 7-day intervals; 75% (82/110) in the treatment group
receiving 1200 mcg of Albuferon at 14-day intervals (p=0.15 vs. Pegasys); 69%
(82/118) in the treatment group receiving 900 mcg of Albuferon at 14-day
intervals (p=0.55 vs. Pegasys); and 53% (62/116) in the treatment group
receiving 1200 mcg of Albuferon at 28-day intervals (p=0.056 vs. Pegasys). Data
also are available on early virologic response at Week 12 (EVR12). (Early
virologic response is defined as a reduction in HCV RNA viral load of at least 2
log -- 99% or greater.) The data show the following percentages of patients
achieving EVR12: 89% (101/114) in the treatment group receiving 180-mcg doses of
Pegasys at 7-day intervals; 90% (99/110) in the treatment group receiving 1200
mcg of Albuferon at 14-day intervals (p=0.73 vs. Pegasys); 84% (99/118) in the
treatment group receiving 900 mcg of Albuferon at 14-day intervals (p=0.30 vs.
Pegasys); and 76% (88/116) in the treatment group receiving 1200 mcg of
Albuferon at 28-day intervals (p=0.011 vs. Pegasys).
Albuferon in combination with ribavirin was well tolerated. The incidence and
duration of flu-like symptoms was similar in all groups, except for a higher
rate of chills in the Albuferon groups. In general, the incidence and severity
of other adverse events was similar across treatment groups, except for a higher
rate of respiratory symptoms (primarily mild cough and dyspnea) in the Albuferon
groups and a higher rate of psychiatric symptoms in the Pegasys group.
Discontinuations due to adverse events were observed by treatment group as
follows: 3 in the 180-mcg 7-day Pegasys cohort (n=114); 8 in the 1200-mcg 14-day
Albuferon cohort (n=110); 3 in the 900-mcg 14-day Albuferon cohort (n=118); and
7 in the 1200-mcg 28-day Albuferon cohort (n=116). There were no
discontinuations due to reductions in hematologic cell counts, which appeared to
be maximal by Week 8, and were well managed with dose reductions in all
treatment groups. The incidence of dose reduction due to hematologic
abnormalities was similar in the Pegasys group and in Albuferon groups
administered every 14 days, but occurred less frequently in the group
administered 1200 mcg Albuferon every 28 days. The rate of emergent antibodies
to interferon was significantly lower in the Albuferon treatment groups (3%)
compared with the Pegasys treatment group (18%) through the first 12 weeks of
treatment (p<0.0001).
HGS also announced that it has completed enrollment, randomization and initial
dosing of 46 patients in a new Phase 2 clinical trial of Albuferon in
combination with ribavirin in treatment-naive patients with genotype 2 or
genotype 3 chronic hepatitis C. The Phase 2 trial is a randomized, open label,
multi-center study being conducted in Canada. Participants have been randomized
into two treatment cohorts, with all patients receiving 1500-mcg doses of
Albuferon in combination with ribavirin for 24 weeks. Albuferon is administered
every 14 days in one cohort and administered every 28 days in the other cohort.
All patients receive oral daily ribavirin at 800 mg in two divided doses. The
primary efficacy endpoint of the Phase 2 study is sustained virologic response
(SVR), defined as undetectable hepatitis C virus (HCV) 24 weeks after completion
of 24 weeks of treatment. Secondary endpoints include rapid virologic response
(undetectable HCV RNA viral load) at Week 4, and safety and quality of life at
Week 24.
Albuferon is a novel, long-acting form of interferon alpha 2b. It is a Human
Genome Sciences drug made possible by the company's proprietary albumin fusion
technology, which was used to improve the pharmacological properties of
interferon alpha. Recombinant interferon alpha is approved for the treatment of
hepatitis C, hepatitis B and a broad range of cancers. Human Genome Sciences is
developing Albuferon for use in the treatment of chronic hepatitis C.
Hepatitis C is an inflammation of the liver caused by the hepatitis C virus. It
is the most common chronic blood-borne infection in the developed world. It is
estimated that as many as 170 million people worldwide are infected with
hepatitis C virus. This includes nearly four million people in the United
States. The hepatitis C virus is transmitted primarily through significant or
repeated exposures to infected blood. Intravenous drug use and sexual contact
with infected persons account for the majority of new hepatitis C infections.
When detectable levels of the hepatitis C virus in the blood persist for at
least six months, a person is diagnosed as having chronic hepatitis C.
CONFERENCE CALL
HGS management will hold a conference call to discuss this announcement today at
10:00 am Eastern Time. Investors may listen to the call by dialing 866/564-7439
or 719/785-9449, passcode 2094807, five to ten minutes before the start of the
call. A replay of the conference call will be available for several days by
dialing 888/203-1112 or 719/457-0820, passcode 2094807. This conference call
also will be webcast. Interested parties who wish to listen to the webcast
should visit the Human Genome Sciences Web site at http://www.hgsi.com/ . The
archive of the conference call will be available several hours after the
conference call and will remain available for several days.
Human Genome Sciences is a company with the mission to discover, develop,
manufacture and market innovative drugs that serve patients with unmet medical
needs, with a primary focus on protein and antibody drugs.
For more information about Albuferon, see
http://www.hgsi.com/products/albuferon.html . Health professionals interested in
more information about trials involving Human Genome Sciences products are
encouraged to inquire via the Contact Us section of the company's Web site,
http://www.hgsi.com/products/request.html , or by calling (301) 610-5790,
extension 3550.
HGS, Human Genome Sciences and Albuferon are trademarks of Human Genome
Sciences, Inc.
This announcement contains forward-looking statements within the meaning of
Section 27A of the Securities Act of 1933, as amended, and Section 21E of the
Securities Exchange Act of 1934, as amended. The forward-looking statements are
based on Human Genome Sciences' current intent, belief and expectations. These
statements are not guarantees of future performance and are subject to certain
risks and uncertainties that are difficult to predict. Actual results may differ
materially from these forward-looking statements because of the Company's
unproven business model, its dependence on new technologies, the uncertainty and
timing of clinical trials, the Company's ability to develop and commercialize
products, its dependence on collaborators for services and revenue, its
substantial indebtedness and lease obligations, its changing requirements and
costs associated with planned facilities, intense competition, the uncertainty
of patent and intellectual property protection, the Company's dependence on key
management and key suppliers, the uncertainty of regulation of products, the
impact of future alliances or transactions and other risks described in the
Company's filings with the Securities and Exchange Commission. Existing and
prospective investors are cautioned not to place undue reliance on these
forward-looking statements, which speak only as of today's date. Human Genome
Sciences undertakes no obligation to update or revise the information contained
in this announcement whether as a result of new information, future events or
circumstances or otherwise.
Footnotes:
1. (HGSI Press Release) Human Genome Sciences Completes Patient
Enrollment in a Phase 2b Clinical Trial of Albuferon in Combination
with Ribavirin in Treatment-Naive Patients with Chronic Hepatitis C.
October 25, 2005.
2. Zeuzem S, Benhamou Y, Shouval D, McHutchison J, Subramanian M, et al.
Interim (week 12) Phase 2b virological efficacy and safety results of
albumin interferon alfa-2b combined with ribavirin in genotype 1
chronic hepatitis C infection. 41st Annual Meeting of the European
Association for the Study of the Liver (EASL), Vienna. Oral
presentation #3088.
3. Rustgi V, Nelson D, Balan V, McHutchison J, Subramanian GM, et al. A
Phase 2 dose-escalation study of Albuferon combined with ribavirin in
non-responders to prior interferon based therapy for chronic hepatitis
C infection. 41st Annual Meeting of the European Association for the
Study of the Liver (EASL), Vienna. Oral presentation #113.
4. (HGSI Press Release) Human Genome Sciences Reports Positive Interim
Results of Phase 2 Clinical Trial of Albuferon in Combination with
Ribavirin in Treatment-Experienced Patients with Chronic Hepatitis C.
March 14, 2006.
5. Nelson DR, et al. A Phase 2 study of Albuferon in combination with
ribavirin in non-responders to prior interferon therapy for chronic
hepatitis C. 56th Annual Meeting of the American Association for the
Study of Liver Diseases (AASLD), 2005. Oral Presentation #204.
6. (HGSI Press Release) Human Genome Sciences Reports Interim Results of
Phase 2 Clinical Trial of Albuferon in Combination with Ribavirin in
Treatment-Experienced Hepatitis C Patients. November 15, 2005
7. Bain VG, Kaita KD, Yoshida EM, McHutchison JG, Subramanian GM, et al.
A Phase 2 study to assess the antiviral activity, safety, and
pharmacokinetics of recombinant human albumin-interferon alfa fusion
protein in genotype 1 chronic hepatitis C patients. Journal of
Hepatology (2006).
8. (HGSI Press Release) Human Genome Sciences Reports Positive Results of
Phase 2 Clinical Trial of Albuferon in Treatment-Naive Patients with
Chronic Hepatitis C. April 14, 2005.
9. Moore P, Balan V, et al. Modulation of interferon specific gene
expression by Albuferon in subjects with chronic hepatitis C and
correlation with anti-viral response. 40th Annual Meeting of the
European Association for the Study of the Liver (EASL), Paris. April
14, 2005. Abstract #447.
10. Balan V, Nelson DR, Sulkowski MS, Subramanian GM, et al. A Phase I/II
study evaluating escalating doses of recombinant human albumin-
interferon-alfa fusion protein in chronic hepatitis C patients who
have failed previous interferon-alfa-based therapy. Antiviral
Therapy, 11:35-45.
11. (HGSI Press Release) Human Genome Sciences Reports Positive Results of
Phase 1/2 Clinical Trial of Albuferon(TM) in Chronic Hepatitis C.
November 2, 2004.
12. Balan V, et al. Molecular profiles of drug response in HCV infected
patients during the first four weeks of therapy for chronic hepatitis
C virus with pegylated interferon containing regimens or Albuferon.
54th Annual Meeting of the American Association for the Study of Liver
Diseases, Boston. October 25, 2003.
13. It is important to note that the method of measurement for dose
determination in the Phase 2b study of Albuferon in combination with
ribavirin in treatment-naive patients (as well as in other Phase 2
studies of the compound) is different from the method of measurement
in the Phase 1/2 study of Albuferon. Accordingly, the 900-mcg dose in
the current study is equivalent to a 680-mcg dose in the Phase 1/2
study, and the 1200-mcg dose is equivalent to 900 mcg in the Phase 1/2
study.
Company News On-Call: http://www.prnewswire.com/comp/121115.html
Website: http://www.hgsi.com/
http://sev.prnewswire.com/biotechnology/20060314/NYTU09514032006-1.html

Hepatitis C Market: Plenty Of Potential, But Little Progress

2006-10-24 18:51:35

Hepatitis C Market: Plenty Of Potential, But Little Progress
BY PETER BENESH
INVESTOR'S BUSINESS DAILY
Posted 3/31/2006
The month of March was not kind to a pair of companies racing to find a cure or
vaccine for hepatitis C, the often fatal liver disease that's been called a
global epidemic by the World Health Organization.
On March 21, Valeant Pharmaceuticals (VRX) said its drug Viramidine, in
combination with current treatments for chronic hepatitis C, had no beneficial
effect. Valeant's stock fell 14% on the news.
Two days later, Idenix, (IDIX) partnering with Novartis, (NVS) said it will
delay the phase two clinical trial of its drug NM283.
Idenix will cut doses from 800 mg to either 400 mg or 200 mg because of
gastrointestinal side effects.
Idenix was subsequently downgraded and watched its shares plummet 28%.
Valeant and Idenix are among several companies trying to find treatments that
are better than the current two-drug standard.
One of those drugs is Ribavirin. It's an oral antiviral sold generically and as
Copegus by Roche and Rebetol by Schering-Plough. (SGP)
The second drug is Pegylated Interferon, a natural human protein that fights
infection.
Pegylated Interferon is sold as Pegasys by Roche and PEG-Intron by
Schering-Plough. It reduces the amount of hepatitis C virus in the blood, but
doesn't eliminate it.
With 4 million Americans infected by hepatitis C, there's an urgent medical
need.
Drug makers also have another incentive to produce a treatment, says analyst
Andrew McDonald of ThinkEquity Partners.
Assuming new drugs come on the market by 2009 or 2010, he predicts the number of
patients needing new hepatitis C drugs will peak in 2011, then trail off through
2016.
"After the debut of new treatment options, more patients will seek treatment,
but at a declining rate (as they get cured)," McDonald said.
"The best treatment - the one that offers the greatest efficacy with the least
amount of patient inconvenience - will be the dominant player. It will likely be
able to command a premium price, with the other therapies left to compete on
price alone."
Taking The Lead
McDonald says the race's current leader is Vertex, (VRTX) with its drug VX-950.
The firm has completed a small phase two trial that was so successful, it's
become "legendary," McDonald said.
Like many drugs targeting hepatitis C, VX-950 is a protease inhibitor. In simple
terms, a protease inhibitor interferes with virus replication.
The trial was 100% successful, says Dr. John Alam, Vertex's chief medical
officer and executive vice president. In the trial, 12 patients took VX-950, an
oral drug, along with Ribavirin and interferon.
"All 12 patients went to undetectable levels of hepatitis C with only four weeks
of treatment," Alam said. "That's a level of response that has not been
approached by any other therapy."
He estimates that $2.5 billion is spent every year in the U.S. and Europe to
battle hepatitis C.
Vertex's only direct competitor is Schering-Plough. Schering's developmental
drug, SCH7, seems to take the same approach as VX-950, analyst McDonald says.
Its success will depend on performance, dosage and side effects.
"Should Schering be unable to achieve similar results, they will likely be at a
significant disadvantage to Vertex," McDonald said.
Vertex could use a win. The company has never turned a profit. Analysts don't
see it moving into the black until 2010 - assuming VX-950 reaches the market.
The firm is about to start a 200-patient phase two trial.
The Food and Drug Administration gave VX-950 a fast-track designation in
December.
Nabi Biopharmaceuticals, (NABI) maker of Civacir, also has the FDA fast-track
designation.
Civacir is aimed at hepatitis C patients who've had liver transplants. These
patients risk reinfection because the virus remains in their blood or elsewhere,
says Nabi Chief Executive Thomas McLain.
Transplant patients are in a bind, he says. "(After transplant), they can't take
interferon and antivirals because of the immuno-suppressive drugs they're on."
Nabi's strategy is to give liver transplant patients antibodies to fight the
remaining hepatitis C virus. The tricky part is getting the antibodies.
The idea is to get those antibodies from the blood of people who are infected
with hepatitis C but are successfully fighting the disease.
"We could collect and purify their antibodies and give them to patients having
transplants," McLain said.
The problem is limited supply. While it might be possible to synthesize
antibodies, hepatitis C mutates. That means it's difficult to come up with a
vaccine.
"