Boceprevir
Encyclopedia
Boceprevir is a protease inhibitor
used as a treatment for hepatitis C
genotype 1. It binds to HCV nonstructural 3 (NS3) active site.
It was being developed by Schering-Plough
, but is now being developed by Merck
since Schering was acquired in 2009. It was approved by the FDA on May 13, 2011.
The phase 2 trial compared 3 different regimens: 4 weeks of peginterferon alfa-2b (1.5 micrograms/kg once weekly) plus ribavirin (800 to 1400 mg daily based on patient weight) followed by boceprevir (800 mg 3 times a day in addition to peginterferon and ribavirin) for 24 weeks or 44 weeks; boceprevir in combination with peginterferon alfa-2b plus ribavirin as above for 28 or 48 weeks (triple therapy); and peginterferon alfa-2b plus low-dose ribavirin (400 to 1000 mg/day) and boceprevir for 48 weeks.
The patients enrolled in the SPRINT-1 study were among the most difficult to treat, and were exclusively those with genotype 1. (The patients were all treatment naive.) Additionally, many of the patients had other difficult-to-treat indices, including cirrhosis (6-9%), high viral load (90%) and African-American ancestry (14-17%). An SVR after 24 weeks off of therapy of 75% was achieved in the group treated for 48 weeks with 4 weeks of lead-in therapy with peginterferon alfa-2b plus ribavirin followed by the addition of boceprivir. This represents a near doubling of the rate of SVR compared to standard therapy without boceprivir in this group.
Anemia was the most common adverse event. It occurred in half of the patients who received boceprivir and by about a third of the patients taking peginterferon alfa-2b plus ribavirin at the standard dose.
The lead investigator of the study was Dr. Paul Kwo, associate professor of medicine at the School of Medicine, Indiana University, in Indianapolis, Indiana, USA.
before being randomized to one of three arms. The first arm received placebo plus peginterferon-ribavirin for 44 weeks, the second arm received boceprevir plus plus peginterferon-ribavirin for 24 weeks, and those with a detectable HCV RNA level between weeks 8 and 24 received placebo plus plus peginterferon-ribavirin for an additional 20 weeks, and the third arm received boceprevir plus plus peginterferon-ribavirin for 44 weeks. Black patients and non-black patients were enrolled and analyzed separately, since black patients have been shown to respond less well to antiviral therapy with peginterferon plus ribavirin than nonblacks. 938 nonblack and 159 black patients were enrolled in the study.
At 44 weeks, among the nonblack cohort, there was a 40% sustained virologic response (125 of 311 patients) in the placebo group, a 67% response (211 of 316 patients) in the response-guided boceprevir group, and a 68% response (214 of 311 patients) in the fixed-duration therapy group. Important side effects included anemia and dysgeusia (distortion of the sense of taste).
403 people were treated in the trial. At 44 weeks, the control group had a lower sustained virologic response rate (21%) than either of the groups treated with boceprevir - 59% sustained viral response for the group with response-guided therapy and 66% response for the group with fixed-duration therapy.
Protease inhibitor (pharmacology)
Protease inhibitors are a class of drugs used to treat or prevent infection by viruses, including HIV and Hepatitis C. PIs prevent viral replication by inhibiting the activity of proteases, e.g.HIV-1 protease, enzymes used by the viruses to cleave nascent proteins for final assembly of new...
used as a treatment for hepatitis C
Hepatitis C
Hepatitis C is an infectious disease primarily affecting the liver, caused by the hepatitis C virus . The infection is often asymptomatic, but chronic infection can lead to scarring of the liver and ultimately to cirrhosis, which is generally apparent after many years...
genotype 1. It binds to HCV nonstructural 3 (NS3) active site.
It was being developed by Schering-Plough
Schering-Plough
Schering-Plough Corporation was a United States-based pharmaceutical company. It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. In 1971, the Schering Corporation merged with Plough to form Schering-Plough. On November 4, 2009 Merck & Co...
, but is now being developed by Merck
Merck & Co.
Merck & Co., Inc. , also known as Merck Sharp & Dohme or MSD outside the United States and Canada, is one of the largest pharmaceutical companies in the world. The Merck headquarters is located in Whitehouse Station, New Jersey, an unincorporated area in Readington Township...
since Schering was acquired in 2009. It was approved by the FDA on May 13, 2011.
SPRINT-1 trial
The SPRINT-1 trial was a phase II trial of Boceprivir in difficult-to-treat patients with HCV genotype 1. Study results were announced at the 44th annual meeting of the European Association for the Study of the Liver in Copenhagen in April, 2009. When used in combination with peginterferon alfa-2b and ribavirin, boceprivir use resulted in significantly higher sustained viral response (SVR) rates in the most difficult-to-treat patients with genotype 1.The phase 2 trial compared 3 different regimens: 4 weeks of peginterferon alfa-2b (1.5 micrograms/kg once weekly) plus ribavirin (800 to 1400 mg daily based on patient weight) followed by boceprevir (800 mg 3 times a day in addition to peginterferon and ribavirin) for 24 weeks or 44 weeks; boceprevir in combination with peginterferon alfa-2b plus ribavirin as above for 28 or 48 weeks (triple therapy); and peginterferon alfa-2b plus low-dose ribavirin (400 to 1000 mg/day) and boceprevir for 48 weeks.
The patients enrolled in the SPRINT-1 study were among the most difficult to treat, and were exclusively those with genotype 1. (The patients were all treatment naive.) Additionally, many of the patients had other difficult-to-treat indices, including cirrhosis (6-9%), high viral load (90%) and African-American ancestry (14-17%). An SVR after 24 weeks off of therapy of 75% was achieved in the group treated for 48 weeks with 4 weeks of lead-in therapy with peginterferon alfa-2b plus ribavirin followed by the addition of boceprivir. This represents a near doubling of the rate of SVR compared to standard therapy without boceprivir in this group.
Anemia was the most common adverse event. It occurred in half of the patients who received boceprivir and by about a third of the patients taking peginterferon alfa-2b plus ribavirin at the standard dose.
The lead investigator of the study was Dr. Paul Kwo, associate professor of medicine at the School of Medicine, Indiana University, in Indianapolis, Indiana, USA.
SPRINT-2 trial
The SPRINT-2 trial was a double-blind study which randomly assigned adults with untreated hepatitis C virus, genotype 1 to one of three groups. Each group received a month of peginterferon alfa-2b and ribavirinRibavirin
Ribavirin is an anti-viral drug indicated for severe RSV infection , hepatitis C infection and other viral infections. Ribavirin is a prodrug, which when metabolised resembles purine RNA nucleotides...
before being randomized to one of three arms. The first arm received placebo plus peginterferon-ribavirin for 44 weeks, the second arm received boceprevir plus plus peginterferon-ribavirin for 24 weeks, and those with a detectable HCV RNA level between weeks 8 and 24 received placebo plus plus peginterferon-ribavirin for an additional 20 weeks, and the third arm received boceprevir plus plus peginterferon-ribavirin for 44 weeks. Black patients and non-black patients were enrolled and analyzed separately, since black patients have been shown to respond less well to antiviral therapy with peginterferon plus ribavirin than nonblacks. 938 nonblack and 159 black patients were enrolled in the study.
At 44 weeks, among the nonblack cohort, there was a 40% sustained virologic response (125 of 311 patients) in the placebo group, a 67% response (211 of 316 patients) in the response-guided boceprevir group, and a 68% response (214 of 311 patients) in the fixed-duration therapy group. Important side effects included anemia and dysgeusia (distortion of the sense of taste).
RESPOND-2 trial
The RESPOND-2 trial studied patients with chronic hepatitis C genotype 1 who did not have a sustained response to therapy with peginterferon-ribavirin therapy. All patients received a month of peg-interferon alfa-2b and ribavirin before being randomized to one of three arms. The first arm received placebo plus peginterferon-ribavirin for 44 weeks. The second group received boceprevir plus peginterferon-ribavirin for 32 weeks, and those with a detectable HCV RNA level at week 8 received peginterferon-ribavirin and placebo for an another 12 weeks. The third group received boceprevir and peginterferon-ribavirin for 44 weeks.403 people were treated in the trial. At 44 weeks, the control group had a lower sustained virologic response rate (21%) than either of the groups treated with boceprevir - 59% sustained viral response for the group with response-guided therapy and 66% response for the group with fixed-duration therapy.