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Positive Interim Data From a Phase 2 Study of INCIVEK™ (telaprevir) Combination Therapy in People Co-Infected with Hepatitis C and HIV Presented at The Liver Meeting®
- Data showed 74% of people had undetectable hepatitis C virus 24 weeks after starting INCIVEK combination treatment -
- Vertex to initiate Phase 3 study to evaluate 24- and 48-week treatment durations in people who are co-infected -
"Treating hepatitis C in people who also have HIV is particularly
challenging as only about 30 percent of people clear the virus after
undergoing nearly a year of treatment with currently available
There are two parts to this study: Part A is evaluating people who are not currently being treated with antiretroviral therapy for HIV infection and Part B is evaluating those who are taking an Atripla® or Reyataz®-based regimen for HIV. This study enrolled patients who were new to hepatitis C treatment. Interim data also showed 63 percent (24/38) of patients treated with INCIVEK combination therapy in this study had an extended rapid hepatitis C viral response (eRVR, measured as undetectable HCV RNA at weeks 4 and 12 of treatment) compared to approximately 5 percent (1/22) who received pegylated-interferon and ribavirin alone.
"Complications associated with hepatitis C such as scarring of the liver
typically develop much faster in people infected with both hepatitis C
and HIV," said
Interim Study Results
Sixty-two people were enrolled in this Phase 2 study and 60 received at least one dose of study drug. This analysis was conducted when all patients had reached week 24 of study treatment (n=44). Sixteen patients discontinued prior to week 24 of study treatment. Reasons for study discontinuation include: meeting a predefined stopping rule (n=6), lost to follow-up (n=1), discontinuation due to hemolytic anemia (n=1), withdrawal of consent (n=2), non-compliance (n=4) and other reasons (n=2).
|24-Week On-Treatment Interim Analysis|
|RVR*||71% (5/7)||0% (0/6)||75% (12/16)||12% (1/8)||60% (9/15)||0% (0/8)||68% (26/38)||4.5% (1/22)|
|eRVR**||57% (4/7)||0% (0/6)||75% (12/16)||12% (1/8)||53% (8/15)||0% (0/8)||63% (24/38)||4.5% (1/22)|
|Week 24 Undetectable||86% (6/7)||33% (2/6)||75% (12/16)||50% (4/8)||67% (10/15)||75% (6/8)||74% (28/38)||55% (12/22)|
Atripla (efavirenz, tenofovir disoproxil fumarate and emtricitabine): TVR was dosed at 1,125 mg, every 8 hours (q8h).
Reyataz-based regimen (ritonavir-boosted atazanavir, tenofovir disoproxil fumarate and emtricitabine or lamivudine): TVR was dosed at 750 mg, every 8 hours (q8h).
*RVR: rapid viral response; undetectable (<25IU/mL undetectable by Roche COBAS Taqman HCV test) at week 4.
**eRVR: early viral response; undetectable (<25IU/mL undetectable by Roche COBAS Taqman HCV test) at weeks 4 and 12.
+12 weeks of telaprevir (TVR), Pegasys® (PEG, pegylated-interferon alfa-2a) and Copegus® (RBV, ribavirin) followed by 36 weeks of only PEG and RBV.
++48 weeks of PEG and RBV only for hepatitis C treatment.
Interim Safety Results
The majority of adverse events in this study were mild or moderate. Adverse events that occurred more frequently (≥10 percent difference) in the INCIVEK arms compared to placebo were abdominal pain, vomiting, nausea, fever, dizziness, depression and itchiness. No severe rashes were reported through 24 weeks. Hyper-bilirubinemia occurred more frequently among patients treated with INCIVEK combination therapy who were also taking a Reyataz-based regimen for the treatment of HIV. Hyper-bilirubinemia is a known side effect of Reyataz-based regimens. Three patients who received INCIVEK combination therapy experienced an adverse event (gall stones, jaundice, hemolytic anemia), all occurring in Part B, that led to discontinuation of one or more study drugs.
About the Ongoing Phase 2 Study
This study is a Phase 2, two-part (A and B), randomized, double-blind, placebo-controlled, parallel group, multi-center study in people chronically infected with both genotype 1 hepatitis C virus and human immunodeficiency virus (HIV) who were new to hepatitis C treatment. The study enrolled 62 people. The primary endpoint of the study is to evaluate the safety and tolerability of telaprevir-based combination therapy in people co-infected with hepatitis C and HIV. A secondary endpoint is to evaluate rates of sustained viral response (SVR, or cure). The study is being conducted by Vertex in collaboration with Tibotec BVBA.
People in Part A and Part B of the study were randomized to receive
either 12 weeks of telaprevir or placebo in combination with
peginterferon alfa-2a (Pegasys®) and ribavirin (Copegus®) followed by 36
weeks of peginterferon alfa-2a and ribavirin alone. Part A (n=13) of the
study enrolled people who were not receiving antiretroviral therapy
(ART) for the treatment of HIV. Part B (n=47) enrolled people who were
being treated for HIV with either Atripla (n=24) or a Reyataz-based
regimen (n=23). For people in Part B who were receiving Atripla,
telaprevir was dosed at 1,125 mg every eight hours (q8h) based on data
from a drug-drug interaction study. For people in Part B who were
receiving a Reyataz-based regimen, telaprevir was dosed at 750 mg every
eight hours (q8h). The ART regimens evaluated in this study were
selected based on current HIV treatment guidelines from the
Vertex's planned Phase 3 study is expected to begin enrollment by the end of 2011. The study will evaluate 24- and 48-week response-guided regimens of INCIVEK combination therapy in people co-infected with hepatitis C and HIV who are new to treatment for hepatitis C or relapsed after at least one prior course of therapy with pegylated-interferon and ribavirin alone. Patients who had not responded to a prior course of treatment (partial responders and nulls) will receive 48 total weeks of INCIVEK-based treatment.
INCIVEK is an oral medicine that acts directly on the hepatitis C virus
protease, an enzyme essential for viral replication. INCIVEK is the most
prescribed direct-acting antiviral for the treatment of genotype 1
chronic hepatitis C and has been used to treat more than 17,000 people
INCIVEK (750 mg) is given as two 375 mg tablets three times daily for 12 weeks in combination with pegylated-interferon and ribavirin. Each monthly package of INCIVEK contains four weekly boxes that include daily blister strips. After the first 12 weeks, all patients stop receiving INCIVEK and continue treatment with pegylated-interferon and ribavirin alone for an additional 12 weeks or 36 weeks of treatment. With INCIVEK combination therapy, more than 60 percent of people treated for the first time, as well as those who relapsed after previous therapy, are expected to complete all treatment in 24 weeks. All other patients receive a total of 48 weeks of treatment. A Phase 3 study evaluating twice-daily dosing of INCIVEK is ongoing.
Rash and anemia are the most serious side effects associated with INCIVEK, which led to treatment discontinuation in about 1 percent of people in clinical studies. The most common side effects reported with INCIVEK combination treatment include fatigue, itching, nausea, diarrhea, vomiting, anal or rectal problems, and taste changes.
Vertex developed telaprevir in collaboration with Tibotec BVBA and
Mitsubishi Tanabe Pharma. Vertex has rights to commercialize telaprevir
IMPORTANT SAFETY INFORMATION
INCIVEK™ (telaprevir) is a prescription medicine used with the medicines peginterferon alfa and ribavirin to treat chronic (lasting a long time) hepatitis C genotype 1 infection in adults with stable liver problems, who have not been treated before or who have failed previous treatment. It is not known if INCIVEK is safe and effective in children under 18 years of age.
Important Safety Information
INCIVEK should always be taken in combination with peginterferon alfa and ribavirin. Ribavirin may cause birth defects or death of an unborn baby. Therefore, a patient should not take INCIVEK combination treatment if she is pregnant or may become pregnant, or if he is a man with a sexual partner who is pregnant. Patients must use two forms of effective birth control during treatment and for the 6 months after treatment with these medicines.
INCIVEK and other medicines can affect each other and can also cause side effects that can be serious or life threatening. There are certain medicines patients cannot take with INCIVEK combination treatment. Patients should tell their healthcare providers about all the medicines they take, including prescription and non-prescription medicines, vitamins and herbal supplements.
INCIVEK can cause serious side effects including rash and anemia. The most common side effects of INCIVEK include itching, nausea, diarrhea, vomiting, anal or rectal problems, taste changes and tiredness. There are other possible side effects of INCIVEK, and side effects associated with peginterferon alfa and ribavirin also apply to INCIVEK combination treatment. Patients should tell their healthcare providers about any side effect that bothers them or doesn't go away.
Please see full Prescribing Information for INCIVEK including the Medication Guide, available at www.INCIVEK.com.
INCIVEK™ is a trademark of
PEGASYS® and COPEGUS® are registered trademarks of Hoffmann-La Roche.
About Hepatitis C
Hepatitis C is a serious liver disease caused by the hepatitis C virus, which is spread through direct contact with the blood of infected people and ultimately affects the liver.1 Chronic hepatitis C can lead to serious and life-threatening liver problems, including liver damage, cirrhosis, liver failure or liver cancer.1 Though many people with hepatitis C may not experience symptoms, others may have symptoms such as fatigue, fever, jaundice and abdominal pain.1
Unlike HIV and hepatitis B virus, chronic hepatitis C can be cured.2 However, approximately 60 percent of people do not achieve SVR,3,4,5 or viral cure,6 after treatment with 48 weeks of pegylated-interferon and ribavirin alone. If treatment is not successful and a person does not achieve a viral cure, they remain at an increased risk for progressive liver disease.7,8
More than 170 million people worldwide are chronically infected with
hepatitis C.6 In
About Hepatitis C and HIV Co-Infection
There are 1 million people living with HIV in
Special Note Regarding Forward-Looking Statements
This press release contains forward-looking statements as defined in the
Private Securities Litigation Reform Act of 1995, including statements
regarding (i) the hope that in the future Vertex will be able to help
more co-infected patients clear the virus; (ii) the possibility that
co-infected patients could have a better chance at a cure for hepatitis
C while maintaining their suppression of HIV; and (iii) the plan to
begin enrollment in a Phase 3 study in people who are co-infected by the
end of 2011. While the company believes the forward-looking statements
contained in this press release are accurate, there are a number of
factors that could cause actual events or results to differ materially
from those indicated by such forward-looking statements. Those risks and
uncertainties include, among other things, that future scientific,
clinical, competitive or other market factors may adversely affect the
potential for INCIVEK-based therapies; that the interim data presented
in this press release may not be predictive of the final outcomes from
this Phase 2 clinical trial; that the outcomes from future clinical
trials of INCIVEK-based therapies in co-infected patients may not be
favorable and the other risks listed under Risk Factors in Vertex's
annual report and quarterly reports filed with the
Vertex creates new possibilities in medicine. Our team discovers, develops and commercializes innovative therapies so people with serious diseases can lead better lives.
Vertex scientists and our collaborators are working on new medicines to cure or significantly advance the treatment of hepatitis C, cystic fibrosis, epilepsy and other life-threatening diseases.
Founded more than 20 years ago in
2 Pearlman BL and
3 Manns MP, McHutchison JG, Gordon SC, et al. Peginterferon alfa-2b plus ribavirin compared with interferon alfa-2b plus ribavirin for initial treatment of chronic hepatitis C: a randomised trial. Lancet. 2001;358:958-965.
4 Fried MW, Shiffman ML, Reddy KR, et al. Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. N Engl J Med. 2002;347:975-982.
5 McHutchison JG, Lawitz EJ, Shiffman ML, et al; IDEAL Study Team. Peginterferon alfa-2b or alfa-2a with ribavirin for treatment of hepatitis C infection. N Engl J Med. 2009;361:580-593.
6 Ghany MG, Strader DB, Thomas DL, Seeff, LB. Diagnosis, management and treatment of hepatitis C; An update. Hepatology. 2009;49 (4):1-40.
7 Morgan TR, Ghany MG, Kim HY, Snow KK, Lindsay K, Lok AS. Outcome of sustained virological responders and non-responders in the Hepatitis C Antiviral Long-Term Treatment Against Cirrhosis (HALT-C) trial. Hepatology. 2008;50(Suppl 4):357A (Abstract 115).
8 Veldt BJ, Heathcote J, Wedmeyer H. Sustained virologic response and clinical outcomes in patients with chronic hepatitis C and advanced fibrosis. Annals of Internal Medicine. 2007; 147: 677-684.
10 Pyenson B, Fitch K,
11 Volk MI, Tocco R, Saini S, Lok, ASF. Public health impact
of antiviral therapy for hepatitis C in
12 Davis GL, Alter MJ,
16 Matthews GV, Dore GJ. HIV and hepatitis C coinfection. JGH. 2008; 23: 1000-1008.
17 Bruno R, Sacchi P, Puoti M, Soriano V, Filice G. HCV chronic hepatitis in patients with HIV: clinical management issues
Am J Gastroenterol 2001; 97:1598—1606.
18 Levin, J. Pegasys/RBV in APRICOT Study- Adherence Improves
SVR 300% in genotype 1. Available at: http://www.natap.org/2005/ICAAC/icaac_31.htm.
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