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NCT00724334 · ClinicalTrials.gov registry record · Phase 1
A Long-Term Study of the Effects of Orally Administered SAR302503 in Patients With Myelofibrosis
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 42
- Enrollment target
NCT00724334: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.
NCT00724334 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. 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
NCT00724334, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 42 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the long-term effects of orally administered SAR302503 (TG101348) in patients with myelofibrosis who have completed the MF-TG101348-001 study.
Interventions
- DRUG SAR302503 (TG101348)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2008-07 |
| Est. Completion | 2014-05 |
| Phase | Phase 1 |
What the finished NCT00724334 record still lists
NCT00724334 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 1 intervention - of which SAR302503 (TG101348) is the first listed.
NCT00724334 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00724334 about?
NCT00724334 is a clinical study titled "A Long-Term Study of the Effects of Orally Administered SAR302503 in Patients With Myelofibrosis". The purpose of this study is to evaluate the long-term effects of orally administered SAR302503 (TG101348) in patients with myelofibrosis who have completed the MF-TG101348-001 study.
What is the current status of trial NCT00724334?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2008-07. Estimated completion is 2014-05.
What interventions are being tested in trial NCT00724334?
The interventions under investigation include: SAR302503 (TG101348) (DRUG).
Who is sponsoring clinical trial NCT00724334?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00724334'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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