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NCT02706795 · ClinicalTrials.gov registry record · Phase 2
Dose-escalating Safety and Preliminary Efficacy of DaxibotulinumtoxinA for Injection in Cervical Dystonia
A Phase 2 study, sponsored by Revance Therapeutics.
- Completed
- Registry status
- Phase 2
- Development phase
- 37
- Enrollment target
NCT02706795: Completed Phase 2 study, sponsored by Revance Therapeutics.
NCT02706795 is a Phase 2 study that has completed, run by Revance Therapeutics. The registered enrollment target is 37 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02706795, a Phase 2 study, has completed, sponsored by Revance Therapeutics.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 37 participants
- Enrollment target
Study Summary
This is an open-label, dose-escalation study to assess the safety and preliminary efficacy of daxibotulinumtoxinA in subjects with isolated cervical dystonia (CD).
Interventions
- BIOLOGICAL DaxibotulinumtoxinA
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2015-09 |
| Est. Completion | 2017-07-17 |
| Phase | Phase 2 |
What the finished NCT02706795 record still lists
NCT02706795 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (72% lower).
The record links to 0 conditions, and to 1 intervention - of which DaxibotulinumtoxinA is the first listed.
NCT02706795 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02706795 about?
NCT02706795 is a clinical study titled "Dose-escalating Safety and Preliminary Efficacy of DaxibotulinumtoxinA for Injection in Cervical Dystonia". This is an open-label, dose-escalation study to assess the safety and preliminary efficacy of daxibotulinumtoxinA in subjects with isolated cervical dystonia (CD).
What is the current status of trial NCT02706795?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 37 participants. The study started on 2015-09. Estimated completion is 2017-07-17.
What interventions are being tested in trial NCT02706795?
The interventions under investigation include: DaxibotulinumtoxinA (BIOLOGICAL).
Who is sponsoring clinical trial NCT02706795?
This trial is sponsored by Revance Therapeutics, which has 27 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02706795's enrollment target sits among peer trials
37 1484th of 2000 higher than 505 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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