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NCT02551185 · ClinicalTrials.gov registry record · Phase 1
ACY 241 in Combination With Paclitaxel in Patients With Advanced Solid Tumors
A Phase 1 study, sponsored by Celgene.
- Completed
- Registry status
- Phase 1
- Development phase
- 20
- Enrollment target
NCT02551185: Completed Phase 1 study, sponsored by Celgene.
NCT02551185 is a Phase 1 study that has completed, run by Celgene. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02551185, a Phase 1 study, has completed, sponsored by Celgene.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 20 participants
- Enrollment target
Study Summary
This is a Phase 1b, multicenter, single arm, open label, dose escalation study to determine the MTD and evaluate the safety and preliminary antitumor activity of orally (PO) administered ACY 241 in combination with intravenously (IV) administered paclitaxel in eligible patients with advanced solid tumors.
Interventions
- DRUG ACY-241
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2015-12-22 |
| Est. Completion | 2019-10-04 |
| Phase | Phase 1 |
What the finished NCT02551185 record still lists
NCT02551185 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).
The record links to 0 conditions, and to 1 intervention - of which ACY-241 is the first listed.
NCT02551185 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02551185 about?
NCT02551185 is a clinical study titled "ACY 241 in Combination With Paclitaxel in Patients With Advanced Solid Tumors". This is a Phase 1b, multicenter, single arm, open label, dose escalation study to determine the MTD and evaluate the safety and preliminary antitumor activity of orally (PO) administered ACY 241 in combination with intravenously (IV) administered paclitaxel in eligible patients with advanced solid t...
What is the current status of trial NCT02551185?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2015-12-22. Estimated completion is 2019-10-04.
What interventions are being tested in trial NCT02551185?
The interventions under investigation include: ACY-241 (DRUG).
Who is sponsoring clinical trial NCT02551185?
This trial is sponsored by Celgene, which has 308 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02551185's enrollment target sits among peer trials
20 1629th of 2000 higher than 285 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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