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ACTIVE NOT RECRUITING Phase 2

Ibrutinib in Treating Patients With Relapsed or Refractory Follicular Lymphoma

NCT01849263 · View on ClinicalTrials.gov ↗

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.

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

FieldValue
Enrollment Target 41 participants
Start Date 2013-04-02
Est. Completion 2026-03-19
Phase Phase 2

Sponsor

National Cancer Institute (NCI)

2,390 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01849263

The ClinicalTrials.gov registry entry for NCT01849263 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Cancer Institute (NCI), which has 2,390 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01849263 reports 13 study locations spanning 8 distinct geographic areas — top geographies include Minnesota, Ontario, Other. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01849263?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Ibrutinib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01849263?

This trial is sponsored by National Cancer Institute (NCI), which has 2,390 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial