FDA
Approves Olysio (simeprevir) for Hepatitis C Virus
November
22, 2013 -- The U.S. Food and Drug Administration today
approved Olysio
(simeprevir), a new therapy to treat chronic hepatitis C virus infection.
Hepatitis C
is a viral disease that causes inflammation of the liver that can lead to
diminished liver function or liver failure. Most people infected with the
hepatitis C virus have no symptoms of the disease until liver damage becomes
apparent, which may take several years. Most of these people then go on to
develop chronic hepatitis C. Some will also develop scarring and poor liver
function (cirrhosis) over many years, which can lead to complications such as
bleeding, jaundice (yellowish eyes or skin), fluid accumulation in the abdomen,
infections or liver cancer. According to the Centers for
Disease Control and Prevention, about 3.2 million Americans are infected
with the hepatitis C virus.
Olysio
is a protease inhibitor that blocks a specific protein needed by the
hepatitis C virus to replicate. It is to be used as a component of a
combination antiviral treatment regimen. In clinical studies, Olysio was
evaluated in combination with peginterferon-alfa and ribavirin, two drugs also
used to treat hepatitis C virus infection. Olysio is intended for adults
with compensated liver disease (a diseased liver that is still functioning),
including cirrhosis, who have not received treatment for their infection
(treatment naïve) or for whom previous treatment has not been effective
(treatment experienced).
“Olysio
is the third FDA-approved protease inhibitor to treat chronic hepatitis C
virus infection, and provides health professionals and patients
with a new, effective treatment for this serious disease,” said Edward Cox,
M.D., director of the Office of Antimicrobial Products in the FDA’s Center for
Drug Evaluation and Research.
In
2011, the FDA approved Victrelis (boceprevir) and Incivek
(telaprevir) for the treatment of hepatitis C. Olysio was reviewed under the
FDA’s priority review program, which provides for an expedited review of drugs
that, if approved, would provide safe and effective therapy when no
satisfactory alternative therapy exists, or offer significant improvement
compared to available therapies.
The
safety and effectiveness of Olysio were evaluated in five clinical studies of
2,026 treatment-naive and treatment-experienced participants randomly
assigned to receive Olysio plus peginterferon-alfa and ribavirin or placebo
plus peginterferon-alfa and ribavirin. The studies were designed to measure
whether a participant’s hepatitis C virus was no longer detected in the blood
at least 12 weeks after finishing treatment (sustained virologic response),
suggesting a participant’s infection had been cured.
Results showed 80 percent of
treatment-naive participants given Olysio plus peginterferon-alfa and ribavirin
achieved sustained virologic response, compared to 50 percent of participants
receiving peginterferon-alfa and ribavirin alone. In one of the studies with
treatment-experienced participants whose infection returned (prior relapsers),
79 percent receiving Olysio plus peginterferon-alfa and ribavirin achieved
sustained virologic response compared to 37 percent of participants receiving
peginterferon-alfa and ribavirin alone.
The
most common side effects reported in clinical study participants
treated with Olysio in combination with peginterferon-alfa and ribavirin were
rash (including photosensitivity), itching (pruritis) and nausea. Serious
photosensitivity reactions resulting in hospitalization were reported. Patients
will be advised to limit sun exposure and to use sun protective measures during
treatment with Olysio in combination with peginterferon alfa and ribavirin. Olysio
should not be used alone to treat chronic hepatitis C infection.
Olysio
is marketed by Janssen Pharmaceuticals, based in Raritan, N.J. Victrelis is
marketed by Whitehouse Station, N.J.-based Merck, and Incivek is marketed by
Cambridge, Mass.-based Vertex Pharmaceuticals.
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