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NCT01779791 · ClinicalTrials.gov registry record · Phase 2
A Study of PCI-32765 (Ibrutinib) in Patients With Refractory Follicular Lymphoma
A Phase 2 study, sponsored by Janssen Research & Development.
- Completed
- Registry status
- Phase 2
- Development phase
- 110
- Enrollment target
NCT01779791: Completed Phase 2 study, sponsored by Janssen Research & Development.
NCT01779791 is a Phase 2 study that has completed, run by Janssen Research & Development. The registered enrollment target is 110 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01779791, a Phase 2 study, has completed, sponsored by Janssen Research & Development.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 110 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the efficacy and safety of PCI-32765 (ibrutinib) administered to patients with chemoimmunotherapy-resistant follicular lymphoma (FL).
Interventions
- DRUG PCI-32765 (Ibrutinib)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2013-04-17 |
| Est. Completion | 2016-05-18 |
| Phase | Phase 2 |
What the finished NCT01779791 record still lists
NCT01779791 is an interventional study that assigns participants to a tested intervention. The registered 110 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% lower).
The record links to 0 conditions, and to 1 intervention - of which PCI-32765 (Ibrutinib) is the first listed.
NCT01779791 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01779791 about?
NCT01779791 is a clinical study titled "A Study of PCI-32765 (Ibrutinib) in Patients With Refractory Follicular Lymphoma". The purpose of this study is to evaluate the efficacy and safety of PCI-32765 (ibrutinib) administered to patients with chemoimmunotherapy-resistant follicular lymphoma (FL).
What is the current status of trial NCT01779791?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 110 participants. The study started on 2013-04-17. Estimated completion is 2016-05-18.
What interventions are being tested in trial NCT01779791?
The interventions under investigation include: PCI-32765 (Ibrutinib) (DRUG).
Who is sponsoring clinical trial NCT01779791?
This trial is sponsored by Janssen Research & Development, which has 593 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01779791's enrollment target sits among peer trials
110 632nd of 2000 higher than 1,361 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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