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NCT00992472 · ClinicalTrials.gov registry record · Phase 1
Bioavailability of Prochlorperazine Suppositories, 25 mg
A Phase 1 study, sponsored by Padagis.
- Completed
- Registry status
- Phase 1
- Development phase
- 42
- Enrollment target
NCT00992472: Completed Phase 1 study, sponsored by Padagis.
NCT00992472 is a Phase 1 study that has completed, run by Padagis. The registered enrollment target is 42 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00992472, a Phase 1 study, has completed, sponsored by Padagis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 42 participants
- Enrollment target
Study Summary
The purpose of this study is to compare prochlorperazine plasma concentrations produced after administration of the test formulation with those produced after administration of a marketed reference product.
Interventions
- DRUG Prochlorperazine suppositories, 25mg
- DRUG Compazine® suppositories, 25mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Phase | Phase 1 |
What the finished NCT00992472 record still lists
NCT00992472 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower).
The record links to 0 conditions, and to 2 interventions - of which Prochlorperazine suppositories, 25mg is the first listed.
NCT00992472 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00992472 about?
NCT00992472 is a clinical study titled "Bioavailability of Prochlorperazine Suppositories, 25 mg". The purpose of this study is to compare prochlorperazine plasma concentrations produced after administration of the test formulation with those produced after administration of a marketed reference product.
What is the current status of trial NCT00992472?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants.
What interventions are being tested in trial NCT00992472?
The interventions under investigation include: Prochlorperazine suppositories, 25mg (DRUG), Compazine® suppositories, 25mg (DRUG).
Who is sponsoring clinical trial NCT00992472?
This trial is sponsored by Padagis, which has 17 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00992472's enrollment target sits among peer trials
42 1105th of 2000 higher than 876 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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