Rituximab, Lenalidomide, and Ibrutinib in Treating Patients With Previously Untreated Stage II-IV Follicular Lymphoma

ClinicalTrials.gov ID: NCT01829568

Public ClinicalTrials.gov record NCT01829568. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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ClinicalTrials.gov public records Last synced Oct 18, 2026, 2:37 PM EDT

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Official title

A Phase I Study of Rituximab, Lenalidomide, and Ibrutinib in Previously Untreated Follicular Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase I trial studies the side effects and best dose of lenalidomide and ibrutinib when given together with rituximab in treating patients with previously untreated stage II-IV follicular lymphoma. Lenalidomide may stimulate the immune system in different ways and stop cancer cells from growing. Ibrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Rituximab is a monoclonal antibody. It binds to a protein called CD20, which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. Giving lenalidomide and ibrutinib together with rituximab may work well in treating follicular lymphoma.

Study identification

NCT ID: NCT01829568
Recruitment status: Active, not recruiting
Study type: Interventional
Phase: Phase 1
Lead sponsor: National Cancer Institute (NCI); NIH
Enrollment: 33 participants

Conditions and interventions

Conditions

Interventions

Ibrutinib Drug
Lenalidomide Drug
Rituximab Biological

Drug · Biological

Eligibility (public fields only)

Age range: 18 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Jun 26, 2013 (Actual)
Primary completion: May 11, 2015 (Actual)
Completion: Jun 6, 2027 (Estimated)
Last update posted: Jun 25, 2026

2013 – 2027

United States locations

U.S. sites: 7
U.S. states: 6
U.S. cities: 7

Facility	City	State	ZIP	Site status
MedStar Georgetown University Hospital	Washington D.C.	District of Columbia	20007	—
University of Chicago Comprehensive Cancer Center	Chicago	Illinois	60637	—
Dana-Farber Cancer Institute	Boston	Massachusetts	02215	—
Roswell Park Cancer Institute	Buffalo	New York	14263	—
NYP/Weill Cornell Medical Center	New York	New York	10065	—
UNC Lineberger Comprehensive Cancer Center	Chapel Hill	North Carolina	27599	—
Ohio State University Comprehensive Cancer Center	Columbus	Ohio	43210	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT01829568, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Jun 25, 2026 · Synced Oct 18, 2026

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The complete public registry record, listed eligibility criteria, and available contact information for NCT01829568 live on ClinicalTrials.gov.

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