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NCT06895356 · ClinicalTrials.gov registry record · Phase 1
A Study to Assess the Relative Bioavailability of Oral Tavapadon in Healthy Adult Participants
A Phase 1 study, sponsored by AbbVie.
- Completed
- Registry status
- Phase 1
- Development phase
- 83
- Enrollment target
NCT06895356: Completed Phase 1 study, sponsored by AbbVie.
NCT06895356 is a Phase 1 study that has completed, run by AbbVie. The registered enrollment target is 83 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06895356, a Phase 1 study, has completed, sponsored by AbbVie.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 83 participants
- Enrollment target
Study Summary
This study will assess the relative bioavailability of two different Oral formulations of tavapadon in healthy adult participants.
Primary Outcome
An adverse event is defined as any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment
Interventions
- DRUG Tavapadon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 83 participants |
| Start Date | 2025-03-26 |
| Est. Completion | 2025-06-16 |
| Phase | Phase 1 |
What the finished NCT06895356 record still lists
NCT06895356 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 83 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% higher).
The record links to 0 conditions, and to 1 intervention - of which Tavapadon is the first listed.
NCT06895356 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06895356 about?
NCT06895356 is a clinical study titled "A Study to Assess the Relative Bioavailability of Oral Tavapadon in Healthy Adult Participants". This study will assess the relative bioavailability of two different Oral formulations of tavapadon in healthy adult participants.
What is the current status of trial NCT06895356?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 83 participants. The study started on 2025-03-26. Estimated completion is 2025-06-16.
What interventions are being tested in trial NCT06895356?
The interventions under investigation include: Tavapadon (DRUG).
Who is sponsoring clinical trial NCT06895356?
This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06895356's enrollment target sits among peer trials
83 665th of 2000 higher than 1,332 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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