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NCT01152671 · ClinicalTrials.gov registry record · Phase 1
A Study of RO5024048 in Japanese and Caucasian Healthy Volunteers
A Phase 1 study, sponsored by Hoffmann-La Roche.
- Completed
- Registry status
- Phase 1
- Development phase
- 97
- Enrollment target
NCT01152671: Completed Phase 1 study, sponsored by Hoffmann-La Roche.
NCT01152671 is a Phase 1 study that has completed, run by Hoffmann-La Roche. The registered enrollment target is 97 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01152671, a Phase 1 study, has completed, sponsored by Hoffmann-La Roche.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 97 participants
- Enrollment target
Study Summary
This randomized, double-blind, placebo-controlled study will assess the safety, tolerability and pharmacokinetics of RO5024048. Japanese and Caucasian healthy volunteers will be randomized to receive either single oral doses of RO5024048 or placebo. Follow-up is 7-10 days.
Interventions
- DRUG Placebo
- DRUG RO5024048
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 97 participants |
| Start Date | 2010-06 |
| Est. Completion | 2010-08 |
| Phase | Phase 1 |
What the finished NCT01152671 record still lists
NCT01152671 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 97 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% higher).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT01152671 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01152671 about?
NCT01152671 is a clinical study titled "A Study of RO5024048 in Japanese and Caucasian Healthy Volunteers". This randomized, double-blind, placebo-controlled study will assess the safety, tolerability and pharmacokinetics of RO5024048. Japanese and Caucasian healthy volunteers will be randomized to receive either single oral doses of RO5024048 or placebo. Follow-up is 7-10 days.
What is the current status of trial NCT01152671?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 97 participants. The study started on 2010-06. Estimated completion is 2010-08.
What interventions are being tested in trial NCT01152671?
The interventions under investigation include: Placebo (DRUG), RO5024048 (DRUG).
Who is sponsoring clinical trial NCT01152671?
This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01152671's enrollment target sits among peer trials
97 597th of 2000 higher than 1,401 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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