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Terminated Phase 1 Interventional Results available

A Study of TAK-659 in Combination With Bendamustine (+/-Rituximab), Gemcitabine, Lenalidomide, or Ibrutinib for the Treatment of Participants With Advanced Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT02954406

Public ClinicalTrials.gov record NCT02954406. 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 Jul 22, 2026, 11:20 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 Phase 1b, Dose Escalation Study to Determine the Recommended Phase 2 Dose of TAK-659 in Combination With Bendamustine (±Rituximab), Gemcitabine, Lenalidomide, or Ibrutinib for the Treatment of Patients With Advanced Non-Hodgkin Lymphoma After At Least 1 Prior Line of Therapy

Study identification

NCT ID
NCT02954406
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Millennium Pharmaceuticals, Inc.
Industry
Enrollment
43 participants

Conditions and interventions

Interventions

  • TAK-659 Drug
  • Bendamustine Drug
  • Rituximab Drug
  • Gemcitabine Drug
  • Lenalidomide Drug
  • Ibrutinib 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
Mar 4, 2017
Primary completion
Jul 26, 2020
Completion
Jul 26, 2020
Last update posted
Feb 17, 2022

2017 – 2020

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
University of Arizona Cancer Center, Tucson Tucson Arizona 85724
University of California San Diego (UCSD) - Moores Cancer Center La Jolla California 92093
Cedars-Sinai Medical Center (CSMC) - Samuel Oschin Comprehensive Cancer Institute West Hollywood California 90048
University of Louisville Kentucky James Graham Brown Cancer Center Louisville Kentucky 40202
Center for Cancer and Blood Disorders Bethesda Maryland 20817
Tufts Medical Center Boston Massachusetts 02111
Henry Ford Hospital Detroit Michigan 48202-2608
NYU Langone Medical Center - NYU Medical Oncology Associates New York New York 10016-4744
University of North Carolina - Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27514
University Hospitals of Cleveland Cleveland Ohio 44106
West Virginia University Morgantown West Virginia 26506

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02954406, 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 Feb 17, 2022 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02954406 live on ClinicalTrials.gov.

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