MedPath

Telaprevir

Generic Name
Telaprevir
Brand Names
-
Drug Type
Small Molecule
Chemical Formula
C36H53N7O6
CAS Number
402957-28-2
Unique Ingredient Identifier
655M5O3W0U
Background

Telaprevir is a direct acting antiviral medication used as part of combination therapy to treat chronic Hepatitis C, an infectious liver disease caused by infection with Hepatitis C Virus (HCV). HCV is a single-stranded RNA virus that is categorized into nine distinct genotypes, with genotype 1 being the most common in the United States, and affecting 72% of all chronic HCV patients . Treatment options for chronic Hepatitis C have advanced significantly since 2011, with the development of Direct Acting Antivirals (DAAs) such as Telaprevir. Telaprevir is an inhibitor of NS3/4A, a serine protease enzyme, encoded by HCV genotype 1 . These enzymes are essential for viral replication and serve to cleave the virally encoded polyprotein into mature proteins like NS4A, NS4B, NS5A and NS5B. The barrier for develoment of resistance to NS3/4A inhibitors is lower than that of NS5B inhibitors, another class of DAAs . Subtitutions at amino acid positions 155, 156, or 168 are known to confer resistance. The substitutions of the enzyme's catalytic triad consisting of H58, D82, and S139 are also likely to alter the affinity of the drug for NS3/4A or the activity of the enzyme itself. Despite this disadvantage Telaprevir is still effective against HCV when paired with Ribavirin, Peginterferon alfa-2a, and Peginterferon alfa-2b.

Telaprevir, Ribavirin, Peginterferon alfa-2a, and Peginterferon alfa-2b were used with the intent to cure, or achieve a sustained virologic response (SVR), after 12 weeks of daily administration of the combination therapy followed by 12 or 36 weeks of therapy with Ribavirin, Peginterferon alfa-2a, and Peginterferon alfa-2b. SVR and eradication of HCV infection is associated with significant long-term health benefits including reduced liver-related damage, improved quality of life, reduced incidence of Hepatocellular Carcinoma, and reduced all-cause mortality .

Telaprevir was available as a fixed dose product (tradename Incivek) used for the treatment of chronic Hepatitis C. Approved in May 2011 by the FDA, Incivek was indicated for the treatment of HCV genotype 1 in combination with Ribavirin, Peginterferon alfa-2a, and Peginterferon alfa-2b . Incivek has since been withdrawn from the market.

Indication

Telaprevir, when used in combination with Ribavirin, Peginterferon alfa-2a, and Peginterferon alfa-2b is indicated for use in the treatment of chronic HCV genotype 1 infection in adults .

Associated Conditions
Chronic Hepatitis C Genotype 1
Associated Therapies
-

A Study Evaluating 24-Week and 48-Week Telaprevir-Based Regimen in Treatment Naïve Subjects With Genotype 1 Chronic Hepatitis C Who Achieve an Extended Rapid Viral Response

Phase 3
Completed
Conditions
Hepatitis C
Interventions
Drug: telaprevir
Drug: ribavirin
Biological: peginterferon alfa-2a
First Posted Date
2008-09-23
Last Posted Date
2021-03-26
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
540
Registration Number
NCT00758043

A Safety and Effectiveness Study of Telaprevir in Chronic, Genotype 1, Hepatitis C Patients That Failed Previous Standard Treatment

Phase 3
Completed
Conditions
Hepatitis C, Chronic
Interventions
Drug: Telaprevir
Drug: Peg-IFN-alfa-2a
Drug: Ribavirin
Drug: Placebo
First Posted Date
2008-06-23
Last Posted Date
2014-01-22
Lead Sponsor
Tibotec BVBA
Target Recruit Count
663
Registration Number
NCT00703118

A Phase 3 Study of Telaprevir in Combination With Pegasys® and Copegus® in Treatment-Naive Subjects With Genotype 1 Hepatitis C Virus (HCV)

Phase 3
Completed
Conditions
Hepatitis C
Interventions
Biological: Pegylated Interferon Alfa 2a
Drug: Ribavirin
Drug: Telaprevir
Other: Placebo
First Posted Date
2008-03-04
Last Posted Date
2014-08-08
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
1095
Registration Number
NCT00627926

An Exploratory Study of Telaprevir in Treatment-Naive Participants With Chronic Genotype 4 Hepatitis C Virus Infection

Phase 2
Completed
Conditions
Hepatitis C
Interventions
Drug: Telaprevir
Drug: Pegylated-interferon-alfa-2a
Drug: Placebo
Drug: Ribavirin
First Posted Date
2007-12-27
Last Posted Date
2013-09-09
Lead Sponsor
Tibotec BVBA
Target Recruit Count
24
Registration Number
NCT00580801

A Phase 2a Study to Evaluate Viral Kinetics and Safety of Telaprevir in Participants With Genotype 2 or 3 Hepatitis C Infection

Phase 2
Completed
Conditions
Hepatitis C, Chronic
Interventions
Drug: Telaprevir
Drug: Peg-IFN-alfa-2a + Ribavirin (Standard Treatment)
Drug: Placebo
First Posted Date
2007-11-20
Last Posted Date
2013-06-17
Lead Sponsor
Tibotec BVBA
Target Recruit Count
52
Registration Number
NCT00561015

A Rollover Study for Subjects Participating in the Control Arm of Study VX06-950-106, VX05-950-104 and VX05-950-104EU Whose Plasma Hepatitis C Virus (HCV) Ribonucleic Acid (RNA) Levels Did Not Respond to Therapy

Phase 2
Completed
Conditions
Hepatitis C
Interventions
Drug: Telaprevir
Drug: Ribavirin
Drug: Pegylated interferon alfa 2a
First Posted Date
2007-09-26
Last Posted Date
2014-08-05
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
117
Registration Number
NCT00535847
Locations
🇺🇸

Atlanta Gastroenterology Associates, Atlanta, Georgia, United States

🇺🇸

South Denver Gastroenterology, Englewood, Colorado, United States

🇺🇸

University of Florida, Gainesville, Florida, United States

and more 38 locations

An Open-Label Study of Telaprevir Administered Every 12 or 8 Hours in Combination With One of Two Pegylated Interferons and Ribavirin in Treatment-Naive Genotype 1 Chronic Hepatitis C Participants

Phase 2
Completed
Conditions
Chronic Hepatitis C
Interventions
First Posted Date
2007-09-12
Last Posted Date
2014-06-25
Lead Sponsor
Tibotec BVBA
Target Recruit Count
166
Registration Number
NCT00528528

A Study of Telaprevir (VX-950), Pegasys and Copegus in Hepatitis C (PROVE3)

Phase 2
Completed
Conditions
Hepatitis C
Interventions
Drug: Telaprevir
Drug: Ribavirin
Drug: Matching Placebo
Drug: Pegylated Interferon Alfa 2a
First Posted Date
2007-01-11
Last Posted Date
2014-08-05
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
465
Registration Number
NCT00420784
Locations
🇺🇸

North Shore University Hospital, Manhasset, New York, United States

🇳🇱

Academic Medical Center, Amsterdam, Netherlands

🇺🇸

University of Florida, Gainesville, Florida, United States

and more 31 locations

Phase 2 Study of VX-950, Pegasys® With and Without Copegus® in Hepatitis C

Phase 2
Completed
Conditions
Chronic Hepatitis C
Interventions
Drug: Ribavirin
Drug: Pegylated Interferon Alfa 2a
Drug: Placebo
Drug: Telaprevir
First Posted Date
2006-09-06
Last Posted Date
2014-07-23
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
334
Registration Number
NCT00372385
Locations
🇬🇧

Call for Information, Call for Information, United Kingdom

🇩🇪

Call For Information, Call For Information, Germany

Phase 2 Study of VX-950, Pegasys®, and Copegus® in Hepatitis C

Phase 2
Completed
Conditions
Chronic Hepatitis C
Interventions
Drug: Telaprevir
Drug: Ribavirin
Drug: Pegylated Interferon Alfa 2a
Other: Placebo
First Posted Date
2006-06-13
Last Posted Date
2014-07-23
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
263
Registration Number
NCT00336479
Locations
🇺🇸

Fox Chase/ Temple Cancer Center, Philadelphia, Pennsylvania, United States

🇺🇸

South Denver Gastroenterology, Englewood, Colorado, United States

🇺🇸

Call for Information, New York, New York, United States

and more 25 locations
© Copyright 2025. All Rights Reserved by MedPath