A Study of PCI-32765 (Ibrutinib) in Patients With Refractory Follicular Lymphoma

PHASE2CompletedINTERVENTIONAL
Enrollment

110

Participants

Timeline

Start Date

April 17, 2013

Primary Completion Date

May 18, 2016

Study Completion Date

May 18, 2016

Conditions
Lymphoma
Interventions
DRUG

PCI-32765 (Ibrutinib)

560 mg capsules administered orally once daily, continuously on a 21-day cycle until progressive disease.

Trial Locations (54)

Unknown

Los Angeles

Stanford

Washington D.C.

Atlanta

Chicago

Westwood

Lexington

Louisville

Baltimore

Detroit

Hackensack

New Brunswick

New York

Greenville

Portland

Philadelphia

Pittsburgh

Houston

Burlington

Seattle

Adelaide

Concord

Melbourne

Milton

Prahran

Courrière

Ghent

Leuven

Créteil

Nice

Nîmes

Paris

Pessac

Pierre-Bénite

Rennes

Cologne

Heidelberg

Mainz

Ulm

Krakow

Warsaw

Wroclaw

Moscow

Nizhny Novgorod

Saint Petersburg

Volgograd

Yekaterinburg

Barcelona

Marbella

Salamanca

Liverpool

London

Manchester

Southampton

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Pharmacyclics LLC.

INDUSTRY

lead

Janssen Research & Development, LLC

INDUSTRY

NCT01779791 - A Study of PCI-32765 (Ibrutinib) in Patients With Refractory Follicular Lymphoma | Biotech Hunter | Biotech Hunter