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NCT01511432 · ClinicalTrials.gov registry record · Phase 1
A Study to Assess the Relative Bioavailability Three New Formulations of Telaprevir in Healthy Subjects
A Phase 1 study, sponsored by Vertex Pharmaceuticals Incorporated.
- Completed
- Registry status
- Phase 1
- Development phase
- 64
- Enrollment target
NCT01511432: Completed Phase 1 study, sponsored by Vertex Pharmaceuticals Incorporated.
NCT01511432 is a Phase 1 study that has completed, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 64 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01511432, a Phase 1 study, has completed, sponsored by Vertex Pharmaceuticals Incorporated.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 64 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the relative bioavailability, safety, and tolerability of 3 new formulations of telaprevir relative to the Incivek 375-mg tablets.
Interventions
- DRUG telaprevir formulation A
- DRUG telaprevir Formulation B
- DRUG telaprevir Formulation C
- DRUG telaprevir Formulation D
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2012-01 |
| Est. Completion | 2012-07 |
| Phase | Phase 1 |
What the finished NCT01511432 record still lists
NCT01511432 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 4 interventions - of which telaprevir formulation A is the first listed.
NCT01511432 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01511432 about?
NCT01511432 is a clinical study titled "A Study to Assess the Relative Bioavailability Three New Formulations of Telaprevir in Healthy Subjects". The purpose of this study is to evaluate the relative bioavailability, safety, and tolerability of 3 new formulations of telaprevir relative to the Incivek 375-mg tablets.
What is the current status of trial NCT01511432?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2012-01. Estimated completion is 2012-07.
What interventions are being tested in trial NCT01511432?
The interventions under investigation include: telaprevir formulation A (DRUG), telaprevir Formulation B (DRUG), telaprevir Formulation C (DRUG), telaprevir Formulation D (DRUG).
Who is sponsoring clinical trial NCT01511432?
This trial is sponsored by Vertex Pharmaceuticals Incorporated, which has 191 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01511432's enrollment target sits among peer trials
64 808th of 2000 higher than 1,181 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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