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NCT00782600 · ClinicalTrials.gov registry record · Phase 1
Study of Controlled Release Formulations of CE-224,535 Against the Immediate Release Formulation in Normal Volunteers
A Phase 1 study, sponsored by Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 16
- Enrollment target
NCT00782600: Completed Phase 1 study, sponsored by Pfizer.
NCT00782600 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00782600, a Phase 1 study, has completed, sponsored by Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 16 participants
- Enrollment target
Study Summary
This study is to test the idea that a controlled release formulation of CE-224,535 may allow for less frequent dosing and exposure to lower levels of drug than an immediate release formulation.
Interventions
- DRUG suspension IR
- DRUG CR 1
- DRUG CR 2
- DRUG CR 3
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 16 participants |
| Start Date | 2008-07 |
| Est. Completion | 2008-08 |
| Phase | Phase 1 |
What the finished NCT00782600 record still lists
NCT00782600 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).
The record links to 0 conditions, and to 4 interventions - of which suspension IR is the first listed.
NCT00782600 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00782600 about?
NCT00782600 is a clinical study titled "Study of Controlled Release Formulations of CE-224,535 Against the Immediate Release Formulation in Normal Volunteers". This study is to test the idea that a controlled release formulation of CE-224,535 may allow for less frequent dosing and exposure to lower levels of drug than an immediate release formulation.
What is the current status of trial NCT00782600?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2008-07. Estimated completion is 2008-08.
What interventions are being tested in trial NCT00782600?
The interventions under investigation include: suspension IR (DRUG), CR 1 (DRUG), CR 2 (DRUG), CR 3 (DRUG).
Who is sponsoring clinical trial NCT00782600?
This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00782600's enrollment target sits among peer trials
16 1786th of 2000 higher than 203 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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