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NCT01053520 · ClinicalTrials.gov registry record · Phase 1
Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female Subjects
A Phase 1 study, sponsored by Abbott.
- Completed
- Registry status
- Phase 1
- Development phase
- 12
- Enrollment target
NCT01053520: Completed Phase 1 study, sponsored by Abbott.
NCT01053520 is a Phase 1 study that has completed, run by Abbott. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01053520, a Phase 1 study, has completed, sponsored by Abbott.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 12 participants
- Enrollment target
Study Summary
This is a Phase 1, randomized, open-label, single center, three period crossover study to determine the oral bioavailability of a new ABT-263 formulation relative to that of the current ABT-263 formulation being administered in ongoing Phase 1/2a studies. Approximately 12 healthy female subjects will be enrolled in this study.
Interventions
- DRUG ABT-263
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2009-10 |
| Est. Completion | 2010-01 |
| Phase | Phase 1 |
What the finished NCT01053520 record still lists
NCT01053520 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).
The record links to 0 conditions, and to 1 intervention - of which ABT-263 is the first listed.
NCT01053520 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01053520 about?
NCT01053520 is a clinical study titled "Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female Subjects". This is a Phase 1, randomized, open-label, single center, three period crossover study to determine the oral bioavailability of a new ABT-263 formulation relative to that of the current ABT-263 formulation being administered in ongoing Phase 1/2a studies. Approximately 12 healthy female subjects wil...
What is the current status of trial NCT01053520?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2009-10. Estimated completion is 2010-01.
What interventions are being tested in trial NCT01053520?
The interventions under investigation include: ABT-263 (DRUG).
Who is sponsoring clinical trial NCT01053520?
This trial is sponsored by Abbott, which has 181 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01053520's enrollment target sits among peer trials
12 1852nd of 2000 higher than 90 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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