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NCT00638313 · ClinicalTrials.gov registry record · Phase 1
Single-Dose Study Of PF-04603629 In Type 2 Diabetic Subjects
A Phase 1 study, sponsored by Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 71
- Enrollment target
NCT00638313: Completed Phase 1 study, sponsored by Pfizer.
NCT00638313 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 71 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00638313, a Phase 1 study, has completed, sponsored by Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 71 participants
- Enrollment target
Study Summary
PF 04603629 is a long acting exendin proposed for the treatment of Type 2 diabetes mellitus. The purpose of this study is to characterize the safety, tolerability, pharmacokinetics and glucose lowering capabilities following a single subcutaneous dose.
Interventions
- BIOLOGICAL Placebo
- BIOLOGICAL PF-04603629
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2007-08 |
| Est. Completion | 2008-02 |
| Phase | Phase 1 |
What the finished NCT00638313 record still lists
NCT00638313 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% higher).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00638313 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00638313 about?
NCT00638313 is a clinical study titled "Single-Dose Study Of PF-04603629 In Type 2 Diabetic Subjects". PF 04603629 is a long acting exendin proposed for the treatment of Type 2 diabetes mellitus. The purpose of this study is to characterize the safety, tolerability, pharmacokinetics and glucose lowering capabilities following a single subcutaneous dose.
What is the current status of trial NCT00638313?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 71 participants. The study started on 2007-08. Estimated completion is 2008-02.
What interventions are being tested in trial NCT00638313?
The interventions under investigation include: Placebo (BIOLOGICAL), PF-04603629 (BIOLOGICAL).
Who is sponsoring clinical trial NCT00638313?
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 NCT00638313's enrollment target sits among peer trials
71 747th of 2000 higher than 1,252 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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