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Drug-Drug Interaction Study Between Telaprevir and Buprenorphine

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Vertex Pharmaceuticals

Status and phase

Completed
Phase 1

Conditions

Hepatitis C
Opioid-Related Disorders

Treatments

Drug: telaprevir
Drug: buprenorphine/naloxone

Study type

Interventional

Funder types

Industry

Identifiers

NCT01275599
VX10-950-024

Details and patient eligibility

About

The purpose of this study is to investigate the drug-drug interaction potential between telaprevir and buprenorphine/naloxone. An understanding of the interaction potential will help to determine whether buprenorphine dose adjustments are necessary for patients who are concomitantly treated with telaprevir.

Telaprevir, in combination with other antiviral agents, is being investigated for the treatment of chronic hepatitis C virus infection. Buprenorphine/naloxone is used for maintainance therapy in patients with opioid dependence.

Enrollment

16 estimated patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males or females between the ages of 18 and 64 years, inclusive. Females must be of non-childbearing potential.
  • Receiving once daily buprenorphine/naloxone maintenance therapy at a stable dose not exceeding 24 mg/6 mg, respectively, for at least 2 weeks prior to screening.

Exclusion criteria

  • Illicit use of drugs such as cocaine, amphetamines and methylenedioxymethamphetamine (MDMA), barbiturates, benzodiazepines, tricyclic antidepressants, methadone or opiates/opioids (apart from buprenorphine).
  • Treatment with any investigational drug within the last 30 days, or 5 half-lives, whichever is longer.
  • Blood donation of 500 mL or more within the last 56 days.
  • Infected with hepatitis B virus, hepatitis C virus, or human immunodeficiency virus (HIV).

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

16 participants in 1 patient group

Open-Label Arm
Experimental group
Description:
The treatment period will include 3 phases: * 14 day run-in period * 7 day co-administration period * 31 day follow-up period
Treatment:
Drug: buprenorphine/naloxone
Drug: telaprevir

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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