ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Study of PCI-32765 (Ibrutinib) in Combination With Either Bendamustine and Rituximab or Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone in Participants With Previously Treated Indolent Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT01974440

Public ClinicalTrials.gov record NCT01974440. 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.

ClinicalTrials.gov public records Last synced May 12, 2026, 2:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of the Bruton's Tyrosine Kinase Inhibitor, PCI-32765 (Ibrutinib), in Combination With Either Bendamustine and Rituximab (BR) or Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Subjects With Previously Treated Indolent Non-Hodgkin Lymphoma (iNHL)

Study identification

NCT ID
NCT01974440
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
403 participants

Conditions and interventions

Conditions

Interventions

  • Bendamustine Drug
  • Cyclophosphamide Drug
  • Doxorubicin Drug
  • PCI-32765 (Ibrutinib) Drug
  • Placebo Drug
  • Prednisone Drug
  • Rituximab Drug
  • Vincristine Drug

Drug

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
Jan 30, 2014
Primary completion
May 29, 2022
Completion
Jun 20, 2023
Last update posted
May 24, 2025

2014 – 2023

United States locations

U.S. sites
32
U.S. states
22
U.S. cities
32
Facility City State ZIP Site status
Not listed Gilbert Arizona
Not listed Campbell California
Not listed Duarte California
Not listed La Jolla California
Not listed Los Angeles California
Not listed Orange California
Not listed Ocala Florida
Not listed Chicago Illinois
Not listed Maywood Illinois
Not listed Indianapolis Indiana
Not listed Westwood Kansas
Not listed Lexington Kentucky
Not listed Lafayette Louisiana
Not listed Scarborough Maine
Not listed Baltimore Maryland
Not listed Bethesda Maryland
Not listed Boston Massachusetts
Not listed Ann Arbor Michigan
Not listed Battle Creek Michigan
Not listed Detroit Michigan
Not listed Saint Louis Park Minnesota
Not listed Denville New Jersey
Not listed New York New York
Not listed Hickory North Carolina
Not listed Pinehurst North Carolina
Not listed Bend Oregon
Not listed Pittsburgh Pennsylvania
Not listed Sioux Falls South Dakota
Not listed Houston Texas
Not listed Lubbock Texas
Not listed Spokane Washington
Not listed Green Bay Wisconsin

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 103 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01974440, 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 May 24, 2025 · Synced May 12, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01974440 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →