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NCT02285647 · ClinicalTrials.gov registry record · Phase 1
An Open-Label, Randomized, Pivotal, Bioequivalence Study of Oral and Intravenous Rolapitant
A Phase 1 study, sponsored by Tesaro.
- Completed
- Registry status
- Phase 1
- Development phase
- 138
- Enrollment target
NCT02285647: Completed Phase 1 study, sponsored by Tesaro.
NCT02285647 is a Phase 1 study that has completed, run by Tesaro. The registered enrollment target is 138 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (130% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02285647, a Phase 1 study, has completed, sponsored by Tesaro.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 138 participants
- Enrollment target
Study Summary
This is an open-label, randomized, single-dose, single-center, parallel-group bioequivalence study of orally- and IV-administered rolapitant in healthy male and female subjects.
Interventions
- DRUG Rolapitant - Oral
- DRUG Rolapitant - IV
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 138 participants |
| Start Date | 2014-09 |
| Est. Completion | 2015-05 |
| Phase | Phase 1 |
What the finished NCT02285647 record still lists
NCT02285647 is an interventional study that assigns participants to a tested intervention. The registered 138 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (130% higher).
The record links to 0 conditions, and to 2 interventions - of which Rolapitant - Oral is the first listed.
NCT02285647 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02285647 about?
NCT02285647 is a clinical study titled "An Open-Label, Randomized, Pivotal, Bioequivalence Study of Oral and Intravenous Rolapitant". This is an open-label, randomized, single-dose, single-center, parallel-group bioequivalence study of orally- and IV-administered rolapitant in healthy male and female subjects.
What is the current status of trial NCT02285647?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 138 participants. The study started on 2014-09. Estimated completion is 2015-05.
What interventions are being tested in trial NCT02285647?
The interventions under investigation include: Rolapitant - Oral (DRUG), Rolapitant - IV (DRUG).
Who is sponsoring clinical trial NCT02285647?
This trial is sponsored by Tesaro, which has 26 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02285647's enrollment target sits among peer trials
138 418th of 2000 higher than 1,581 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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