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NCT01849263 · ClinicalTrials.gov registry record · Phase 2
Ibrutinib in Treating Patients With Relapsed or Refractory Follicular Lymphoma
A Phase 2 study of Recurrent Grade 1 Follicular Lymphoma and Recurrent Grade 2 Follicular Lymphoma, sponsored by National Cancer Institute (NCI).
- Active
- Registry status
- Phase 2
- Development phase
- 41
- Enrollment target
- 13
- Study locations
NCT01849263: Active Phase 2 study of Recurrent Grade 1 Follicular Lymphoma and Recurrent Grade 2 Follicular Lymphoma, sponsored by National Cancer Institute (NCI).
NCT01849263 is a Phase 2 study of Recurrent Grade 1 Follicular Lymphoma and Recurrent Grade 2 Follicular Lymphoma that is active but no longer recruiting, run by National Cancer Institute (NCI). The registered enrollment target is 41 participants, above the 35-participant average among 11 other Recurrent Grade 1 Follicular Lymphoma trials with a reported enrollment target (17% higher). The trial reports 13 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01849263, a Phase 2 study of Recurrent Grade 1 Follicular Lymphoma and Recurrent Grade 2 Follicular Lymphoma, is active but no longer recruiting, sponsored by National Cancer Institute (NCI).
- ACTIVE NOT RECRUITING
- Registry status
- Phase 2
- Development phase
- 41 participants
- Enrollment target
- 13
- Study locations
Study Summary
This phase II trial studies how well ibrutinib works in treating patients with follicular lymphoma that has come back after a period of improvement or does not respond to treatment. Ibrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.
Primary Outcome
Overall response rate defined as a partial response (PR) or complete response (CR) as the objective status at any time during treatment, evaluated using the Cheson et al. Revised Response Criteria for Malignant Lymphoma. Ninety-five percent binomial confidence intervals for the true success proportion will be calculated. A CR is defined as the disappearance of all evidence of disease. A PR is defined as ≥ 50% decrease in the sum of the products of dimensions (SPD) of up to 6 largest dominant ma
Conditions Studied
Interventions
- OTHER Laboratory Biomarker Analysis
- DRUG Ibrutinib
Study Locations (13)
Minnesota
- Mayo Clinic in Rochester - Rochester
- Metro Minnesota Community Oncology Research Consortium - Saint Louis Park
- Park Nicollet Clinic - Saint Louis Park - Saint Louis Park
Ontario
- Juravinski Cancer Centre at Hamilton Health Sciences - Hamilton
- Kingston Health Sciences Centre - Kingston
- University Health Network-Princess Margaret Hospital - Toronto
Other
- National University Hospital Singapore - Singapore
- National Cancer Centre Singapore - Singapore
Arizona
- Mayo Clinic in Arizona - Scottsdale
Florida
- Mayo Clinic in Florida - Jacksonville
Missouri
- Washington University School of Medicine - St Louis
Pennsylvania
- Fox Chase Cancer Center - Philadelphia
Wisconsin
- University of Wisconsin Carbone Cancer Center - University Hospital - Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 41 participants |
| Start Date | 2013-04-02 |
| Est. Completion | 2026-03-19 |
| Phase | Phase 2 |
What the registry record for NCT01849263 still lists
NCT01849263 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, above the 35-participant average among 11 other Recurrent Grade 1 Follicular Lymphoma trials with a reported enrollment target (17% higher).
The record links to 5 conditions, with Recurrent Grade 1 Follicular Lymphoma appearing as the primary indexed condition, and to 2 interventions - of which Laboratory Biomarker Analysis is the first listed.
NCT01849263 lists 13 locations in 8 states (Minnesota, Ontario, Other).
Frequently Asked Questions
What is clinical trial NCT01849263 about?
NCT01849263 is a clinical study titled "Ibrutinib in Treating Patients With Relapsed or Refractory Follicular Lymphoma". This phase II trial studies how well ibrutinib works in treating patients with follicular lymphoma that has come back after a period of improvement or does not respond to treatment. Ibrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.
What is the current status of trial NCT01849263?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 41 participants. The study started on 2013-04-02. Estimated completion is 2026-03-19.
What conditions does trial NCT01849263 study?
This clinical trial studies the following conditions: Recurrent Grade 1 Follicular Lymphoma, Recurrent Grade 2 Follicular Lymphoma, Grade 3a Follicular Lymphoma, Refractory Follicular Lymphoma, Recurrent Grade 3 Follicular Lymphoma.
What interventions are being tested in trial NCT01849263?
The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Ibrutinib (DRUG).
Who is sponsoring clinical trial NCT01849263?
This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01849263 being conducted?
This trial has 13 study locations across Arizona, Florida, Minnesota, Missouri, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Recurrent Grade 1 Follicular Lymphoma
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01849263's enrollment target sits among peer trials
41 4th of 11 higher than 7 of 11 other Recurrent Grade 1 Follicular Lymphoma trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Recurrent Grade 1 Follicular Lymphoma 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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