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NCT00540878 · ClinicalTrials.gov registry record · Phase 1
A Study to Estimate the Effect of Formulation on the Relative Absorption of SB-751689 Administered to Healthy Women
A Phase 1 study, sponsored by GlaxoSmithKline.
- Completed
- Registry status
- Phase 1
- Development phase
- 25
- Enrollment target
NCT00540878: Completed Phase 1 study, sponsored by GlaxoSmithKline.
NCT00540878 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00540878, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 25 participants
- Enrollment target
Study Summary
This study will examine the effects of formulation on the relative bioavailability of SB-751689 (400 mg) administered to healthy postmenopausal women. Subjects will receive a single oral dose of each formulation, with five formulations of SB-751689 tested in total. Blood samples will be taken up to 24 hours postdose after each dose administration. This study will provide information for future possible formulation development of SB-751689 for Phase III.
Interventions
- DRUG SB-751689 oral tablets (400 mg)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2007-04 |
| Phase | Phase 1 |
What the finished NCT00540878 record still lists
NCT00540878 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).
The record links to 0 conditions, and to 1 intervention - of which SB-751689 oral tablets (400 mg) is the first listed.
NCT00540878 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00540878 about?
NCT00540878 is a clinical study titled "A Study to Estimate the Effect of Formulation on the Relative Absorption of SB-751689 Administered to Healthy Women". This study will examine the effects of formulation on the relative bioavailability of SB-751689 (400 mg) administered to healthy postmenopausal women. Subjects will receive a single oral dose of each formulation, with five formulations of SB-751689 tested in total. Blood samples will be taken up to ...
What is the current status of trial NCT00540878?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2007-04.
What interventions are being tested in trial NCT00540878?
The interventions under investigation include: SB-751689 oral tablets (400 mg) (DRUG).
Who is sponsoring clinical trial NCT00540878?
This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00540878's enrollment target sits among peer trials
25 1495th of 2000 higher than 481 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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