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NCT00547560 · ClinicalTrials.gov registry record · Phase 1
Study Evaluating Multiple Doses Of GSI-953 Within The Elderly Population
A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 49
- Enrollment target
NCT00547560: Completed Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
NCT00547560 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 49 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00547560, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 49 participants
- Enrollment target
Study Summary
To assess the safety and tolerability of ascending, multiple, oral doses of GSI-953 in healthy elderly subjects.
Interventions
- DRUG GSI-953
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 49 participants |
| Start Date | 2007-08 |
| Est. Completion | 2009-10 |
| Phase | Phase 1 |
What the finished NCT00547560 record still lists
NCT00547560 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower).
The record links to 0 conditions, and to 1 intervention - of which GSI-953 is the first listed.
NCT00547560 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00547560 about?
NCT00547560 is a clinical study titled "Study Evaluating Multiple Doses Of GSI-953 Within The Elderly Population". To assess the safety and tolerability of ascending, multiple, oral doses of GSI-953 in healthy elderly subjects.
What is the current status of trial NCT00547560?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2007-08. Estimated completion is 2009-10.
What interventions are being tested in trial NCT00547560?
The interventions under investigation include: GSI-953 (DRUG).
Who is sponsoring clinical trial NCT00547560?
This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00547560's enrollment target sits among peer trials
49 1017th of 2000 higher than 976 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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