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Completed Phase 2 Interventional

A Study to Evaluate the Efficacy and Safety of Ibrutinib, in Patients With Mantle Cell Lymphoma Who Progress After Bortezomib Therapy

ClinicalTrials.gov ID: NCT01599949

Public ClinicalTrials.gov record NCT01599949. 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 4, 2026, 7:12 AM 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 2, Multicenter, Single-Arm, Study to Evaluate the Efficacy and Safety of Single-Agent Bruton's Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Subjects With Mantle Cell Lymphoma Who Progress After Bortezomib Therapy

Study identification

NCT ID
NCT01599949
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
120 participants

Conditions and interventions

Interventions

  • 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
Jul 31, 2012
Primary completion
Apr 30, 2015
Completion
Apr 30, 2015
Last update posted
May 31, 2016

2012 – 2015

United States locations

U.S. sites
32
U.S. states
23
U.S. cities
32
Facility City State ZIP Site status
Not listed La Jolla California
Not listed Los Angeles California
Not listed Stanford California
Not listed Norwalk Connecticut
Not listed Jacksonville Florida
Not listed Chicago Illinois
Not listed Peoria Illinois
Not listed Goshen Indiana
Not listed Iowa City Iowa
Not listed Sioux City Iowa
Not listed Westwood Kansas
Not listed Lexington Kentucky
Not listed Louisville Kentucky
Not listed Metairie Louisiana
Not listed Baltimore Maryland
Not listed Boston Massachusetts
Not listed Worcester Massachusetts
Not listed Ann Arbor Michigan
Not listed Detroit Michigan
Not listed Jefferson City Missouri
Not listed St Louis Missouri
Not listed Omaha Nebraska
Not listed Hackensack New Jersey
Not listed New York New York
Not listed Syracuse New York
Not listed Watertown South Dakota
Not listed Nashville Tennessee
Not listed Houston Texas
Not listed Burlington Vermont
Not listed Charlottesville Virginia
Not listed Morgantown West Virginia
Not listed Madison 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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01599949, 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 31, 2016 · Synced May 4, 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 NCT01599949 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →