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NCT00384280

An Open Label, 2-period, Sequential Study to Determine the Impact of Multiple Doses of Rifampin on Single-dose Pharmacokinetics of HCV-796

Completed Phase 1 Last updated 10 August 2009
What this trial tests

Phase 1 trial testing Rifampin in Healthy in 24 participants. Completed in 1 November 2006.

Timeline
1 September 2006
Primary endpoint
1 November 2006
1 November 2006

Quick facts

Lead sponsorWyeth is now a wholly owned subsidiary of Pfizer
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment24
Start date1 September 2006
Primary completion1 November 2006
Estimated completion1 November 2006

Drugs / interventions tested

Conditions studied

Sponsor

Wyeth is now a wholly owned subsidiary of Pfizer — full company profile →

Who can join

Adults 18 to 50, any sex, with Healthy. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

An open label, 2-period, sequential study to determine the impact of multiple doses of rifampin on single-dose pharmacokinetics of HCV-796

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Rifampin

Trials testing the same drug.

Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Wyeth is now a wholly owned subsidiary of Pfizer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00384280.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing