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 Incivek has since been withdrawn from the market.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

Efficacy and Safety of Therapy Against HCV Based on Direct-acting Antivirals in Real-life Conditions

First Posted Date
2015-01-07
Last Posted Date
2022-06-29
Lead Sponsor
Valme University Hospital
Target Recruit Count
1128
Registration Number
NCT02333292
Locations
🇪🇸

Valme University Hospital, Seville, Andalusia, Spain

Comparative Effectiveness and Tolerability of Boceprevir vs Telaprevir

Not Applicable
Completed
Conditions
Hepatitis C, Chronic
Cirrhosis
Interventions
First Posted Date
2014-04-14
Last Posted Date
2017-03-15
Lead Sponsor
Louis Stokes VA Medical Center
Target Recruit Count
50
Registration Number
NCT02113631
Locations
🇺🇸

Louis Stokes Cleveland VA medical center, Cleveland, Ohio, United States

Telaprevir in Genotype 3 HCV

Phase 4
Completed
Conditions
Hepatitis C
Interventions
Drug: 40 Kd Pegylated interferon alfa 2a
First Posted Date
2014-03-14
Last Posted Date
2023-01-05
Lead Sponsor
Queen Mary University of London
Target Recruit Count
14
Registration Number
NCT02087111
Locations
🇬🇧

Nottingham University Hospitals Trust, Nottingham, United Kingdom

🇬🇧

Bradford Teaching Hospitals NHS Foundation Trust, Bradford, United Kingdom

🇬🇧

Ste Georges Healthcare NHS Trust, London, United Kingdom

and more 1 locations

Open Label Trial of PEG-IFN, RBV & TVR vs. PEG-IFN & RBV Alone in Tx of HCV-1 in HIV-1 Co-infected Patients (CHAT)

Phase 3
Completed
Conditions
HIV
Interventions
First Posted Date
2013-12-10
Last Posted Date
2017-04-12
Lead Sponsor
St Stephens Aids Trust
Target Recruit Count
20
Registration Number
NCT02006745
Locations
🇬🇧

St Stephens AIDS Trust, London, United Kingdom

Open-Label Safety Study of Telaprevir and Sofosbuvir in Chronic Hepatitis C Genotype 1

Phase 2
Completed
Conditions
Hepatitis C, Chronic
Interventions
First Posted Date
2013-11-25
Last Posted Date
2018-04-23
Lead Sponsor
University of Florida
Target Recruit Count
20
Registration Number
NCT01994486
Locations
🇺🇸

UF Hepatology Research at CTRB, Gainesville, Florida, United States

Vitamin D + Telaprevir + Peginterferon + Ribavirin for of Hepatitis C Genotype 1

Phase 2
Withdrawn
Conditions
Hepatitis C
Interventions
First Posted Date
2013-07-02
Last Posted Date
2014-05-14
Lead Sponsor
Timothy Morgan, MD
Registration Number
NCT01890772
Locations
🇺🇸

Minneapolis VAHCS, Minneapolis, Minnesota, United States

🇺🇸

VA Long Beach Healthcare System, Long Beach, California, United States

🇺🇸

Kansas City VA Medical Center, Kansas City, Missouri, United States

and more 1 locations

Miravirsen in Combination With Telaprevir and Ribavirin in Null Responder to Pegylated-Interferon Alpha Plus Ribavirin Subjects With Chronic Hepatitis C Virus Infection

Phase 2
Conditions
Hepatitis C, Chronic
Interventions
First Posted Date
2013-06-07
Last Posted Date
2014-11-18
Lead Sponsor
Santaris Pharma A/S
Target Recruit Count
20
Registration Number
NCT01872936
Locations
🇺🇸

Research Specialists of Texas, Houston, Texas, United States

🇺🇸

The Liver Institute at Methodist Dallas Medical Center, Dallas, Texas, United States

🇵🇷

Fundacion de Investigacion de Diego, San Juan, Puerto Rico

Open Label Trial to Compare BI 207127 to Telaprevir in HCV Patients

Phase 3
Withdrawn
Conditions
Hepatitis C, Chronic
Interventions
First Posted Date
2013-05-21
Last Posted Date
2014-01-23
Lead Sponsor
Boehringer Ingelheim
Registration Number
NCT01858961
Locations
🇦🇺

1241.37.61002 Boehringer Ingelheim Investigational Site, Westmead, New South Wales, Australia

🇸🇪

1241.37.46001 Boehringer Ingelheim Investigational Site, Stockholm, Sweden

🇪🇸

1241.37.34003 Boehringer Ingelheim Investigational Site, Madrid, Spain

and more 9 locations

A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compared With Telaprevir (a Licensed Product) for Treatment of Chronic Hepatitis C Infection in Treatment-experienced Adults

Phase 3
Completed
Conditions
Chronic Hepatitis C Infection
Interventions
Drug: ABT-450/r/ABT-267, ABT-333
Drug: Pegylated Interferon a-2a (PegINF)
First Posted Date
2013-05-15
Last Posted Date
2018-06-06
Lead Sponsor
AbbVie
Target Recruit Count
148
Registration Number
NCT01854528

A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compared With Telaprevir (a Licensed Product) in People With Hepatitis C Virus Infection Who Have Not Had Treatment Before

Phase 3
Completed
Conditions
Chronic Hepatitis C Infection
Interventions
Drug: ABT-450/r/ABT-267, ABT-333
Drug: Pegylated Interferon alpha 2-a (PegIFN)
First Posted Date
2013-05-15
Last Posted Date
2018-06-06
Lead Sponsor
AbbVie
Target Recruit Count
311
Registration Number
NCT01854697
© Copyright 2025. All Rights Reserved by MedPath