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 Incivek has since been withdrawn from the market.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

Interaction Between Paroxetine and Telaprevir

Phase 2
Terminated
Conditions
Hepatitis C Infection
Depression
Interventions
First Posted Date
2013-04-26
Last Posted Date
2020-12-08
Lead Sponsor
Radboud University Medical Center
Target Recruit Count
3
Registration Number
NCT01841502
Locations
🇳🇱

Academic Medical Centre Amsterdam, Amsterdam, Netherlands

🇳🇱

Reinier de Graaf Groep, Delft, Netherlands

🇳🇱

University Medical Centre Groningen, Groningen, Netherlands

and more 4 locations

Telaprevir Plus Standard of Care (SOC) in HCV Associated Hepatocellular Carcinoma (HCC)

Phase 3
Terminated
Conditions
Infection
Interventions
Drug: Pegylated Interferon Alfa 2a
First Posted Date
2013-04-01
Last Posted Date
2020-09-24
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
1
Registration Number
NCT01821963
Locations
🇺🇸

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Pharmacokinetic Interactions Between Telaprevir and Un-boosted Atazanavir

Phase 1
Completed
Conditions
Hepatitis C, Chronic
HIV Infection
Interventions
First Posted Date
2013-03-27
Last Posted Date
2013-04-22
Lead Sponsor
Hospitales Universitarios Virgen del Rocío
Target Recruit Count
14
Registration Number
NCT01818856
Locations
🇪🇸

Hospital Universitario Virgen del Rocio, Seville, Spain

A Drug Interaction Study of the Effects of PPI-668 on the Pharmacokinetics of Midazolam and Omeprazole

Phase 1
Completed
Conditions
Pharmacokinetic Assessments in Healthy Volunteers
Interventions
First Posted Date
2013-02-08
Last Posted Date
2013-03-26
Lead Sponsor
Presidio Pharmaceuticals, Inc.
Target Recruit Count
24
Registration Number
NCT01786382
Locations
🇺🇸

Spaulding Clinical Research, West Bend, Wisconsin, United States

Clinical Pharmacology Study of MP-424

Phase 1
Completed
Conditions
Chronic Hepatitis C
Interventions
First Posted Date
2013-01-11
Last Posted Date
2017-01-26
Lead Sponsor
Mitsubishi Tanabe Pharma Corporation
Target Recruit Count
26
Registration Number
NCT01766167

Hepatitis C Virus Post-Exposure Prophylaxis for Health Care Workers

Phase 4
Withdrawn
Conditions
Viral Hepatitis C
Interventions
First Posted Date
2013-01-11
Last Posted Date
2014-08-13
Lead Sponsor
Massachusetts General Hospital
Registration Number
NCT01766115
Locations
🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

Efficacy and Safety of MP-424, Peginterferon Alfa-2a (PEG-IFN Alfa-2a), and Ribavirin(RBV) in Treatment-Naïve or Relapsed Hepatitis C

Phase 3
Completed
Conditions
Chronic Hepatitis C (CHC)
Interventions
First Posted Date
2012-12-20
Last Posted Date
2016-10-03
Lead Sponsor
Mitsubishi Tanabe Pharma Corporation
Target Recruit Count
54
Registration Number
NCT01753557
Locations
🇯🇵

Toranomon Hospital, Kawasaki City, Takatsu-ku, Japan

Efficacy and Safety of MP-424, Interferon Beta (IFN Beta), and Ribavirin(RBV) in Treatment-Naïve or Having Received Interferon Based Therapy With Chronic Hepatitis C (CHC)

Phase 3
Completed
Conditions
Chronic Hepatitis C(CHC)
Interventions
Drug: RBV(48 weeks)
Drug: IFN beta(48 weeks)
Drug: RBV(24 weeks)
Drug: IFN beta(24 weeks)
First Posted Date
2012-12-20
Last Posted Date
2018-10-26
Lead Sponsor
Mitsubishi Tanabe Pharma Corporation
Target Recruit Count
74
Registration Number
NCT01753570
Locations
🇯🇵

Toranomon Hospital, Kawasaki City, Takatsu-ku, Japan

A Phase 3, Comparative Study of Asunaprevir and Daclatasvir Combination Therapy Versus Telaprevir Therapy in Japanese HCV Subjects

Phase 3
Completed
Conditions
Hepatitis C Virus Infection
Interventions
First Posted Date
2012-10-31
Last Posted Date
2015-10-09
Lead Sponsor
Bristol-Myers Squibb
Target Recruit Count
258
Registration Number
NCT01718145
Locations
🇯🇵

Local Institution, Saitama, Japan

Efficacy and Safety Evaluation of a Regimen Consisting of Peginterferon Lambda-1a + Ribavirin + Daclatasvir (Lambda + RBV + DCV) in HCV Genotype 1b Treatment naïve Patients or Prior Relapsers to Peginterferon Alfa + Ribavirin (Alfa + RBV) Therapy

Phase 3
Completed
Conditions
Hepatitis C
Interventions
Biological: Peginterferon Alfa-2a
Biological: Peginterferon Lambda-1a
First Posted Date
2012-10-31
Last Posted Date
2015-10-09
Lead Sponsor
Bristol-Myers Squibb
Target Recruit Count
444
Registration Number
NCT01718158
Locations
🇺🇸

Nashville Medical Research Institute, Nashville, Tennessee, United States

🇺🇸

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

🇬🇧

Local Institution, London, Greater London, United Kingdom

and more 6 locations
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