MedPath

Telaprevir

Generic Name
Telaprevir
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 Incivek has since been withdrawn from the market.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

Viral Kinetics in HCV Clearance in Subjects With Hemophilia

Phase 1
Completed
Conditions
Chronic Hepatitis C
Hemophilia
Interventions
First Posted Date
2012-10-11
Last Posted Date
2015-04-06
Lead Sponsor
Kenneth Sherman
Target Recruit Count
5
Registration Number
NCT01704521
Locations
🇺🇸

UC Physicians Company, Cincinnati, Ohio, United States

An Open-Label Study of the Effect of Telaprevir in Combination With Peginterferon Alfa-2b and Ribavirin in Pediatric Subjects Infected With Hepatitis C Virus

Phase 1
Terminated
Conditions
Hepatitis C
Interventions
First Posted Date
2012-10-04
Last Posted Date
2016-07-20
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
42
Registration Number
NCT01701063

Eltrombopag/Boceprevir and Eltrombopag/Telaprevir Drug-Drug Interaction Study In Healthy Adult Subjects

Phase 1
Completed
Conditions
Thrombocytopaenia
Interventions
First Posted Date
2012-08-06
Last Posted Date
2017-11-13
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
56
Registration Number
NCT01657552
Locations
🇺🇸

GSK Investigational Site, Baltimore, Maryland, United States

Dose Ranging of GSK2336805 in Combination Therapy

Phase 2
Completed
Conditions
Hepatitis C, Chronic
Interventions
Drug: GSK2336805 40 mg
Drug: GSK2336805 60 mg
First Posted Date
2012-07-24
Last Posted Date
2017-06-02
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
286
Registration Number
NCT01648140
Locations
🇵🇷

GSK Investigational Site, San Juan, Puerto Rico

Drug Interaction Study to Assess the Effect of Co-Administered Miravirsen and Telaprevir in Healthy Subjects

Phase 1
Completed
Conditions
Hepatitis C
Chronic Hepatitis C
Interventions
First Posted Date
2012-07-20
Last Posted Date
2012-11-12
Lead Sponsor
Santaris Pharma A/S
Target Recruit Count
5
Registration Number
NCT01646489
Locations
🇺🇸

Spaulding Clinical Research, West Bend, Wisconsin, United States

A Study to Investigate the Potential Pharmacokinetic Interactions Between Phenytoin or Carbamazepine and Telaprevir

Phase 1
Completed
Conditions
Healthy Participants
Interventions
First Posted Date
2012-07-10
Last Posted Date
2013-10-24
Lead Sponsor
Janssen Infectious Diseases BVBA
Target Recruit Count
24
Registration Number
NCT01635829

A Study to Assess Safety and Pharmacokinetics of Telaprevir in Patients With Hepatic Impairment

Phase 1
Completed
Conditions
Hepatic Impairment
Interventions
First Posted Date
2012-05-17
Last Posted Date
2013-11-11
Lead Sponsor
Janssen Infectious Diseases BVBA
Target Recruit Count
24
Registration Number
NCT01600976

Phase 3 Efficacy and Safety Study of Peginterferon Lambda-1a and Ribavirin With Telaprevir

Phase 3
Completed
Conditions
Hepatitis C Virus
Interventions
Biological: Peginterferon Lambda-1a
Biological: Peginterferon Alfa-2a
First Posted Date
2012-05-15
Last Posted Date
2019-07-31
Lead Sponsor
Bristol-Myers Squibb
Target Recruit Count
881
Registration Number
NCT01598090
Locations
🇨🇦

Hopital Maisonneuve-Rosemont, Montreal, Quebec, Canada

🇺🇸

Cedars Sinai Medical Center, Los Angeles, California, United States

🇺🇸

Mercy Medical Center, Baltimore, Maryland, United States

and more 32 locations

Pegylated Interferon, Ribavirin, Telaprevir in Hepatitis C Virus Infection in Orthotopic Liver Transplant Recipients

Phase 4
Terminated
Conditions
Hepatitis C
Interventions
First Posted Date
2012-05-04
Last Posted Date
2016-06-15
Lead Sponsor
University of Chicago
Target Recruit Count
3
Registration Number
NCT01592006
Locations
🇺🇸

University of Chicago Medical Center, Chicago, Illinois, United States

VX-222 + Telaprevir + Ribavirin for 12 or 16 Weeks in Treatment-Naive Subjects With Genotype 1a Hepatitis C

Phase 2
Completed
Conditions
Chronic Hepatitis C Virus
Interventions
First Posted Date
2012-04-20
Last Posted Date
2014-07-04
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Target Recruit Count
64
Registration Number
NCT01581138
© Copyright 2025. All Rights Reserved by MedPath