A Study of the Bruton's Tyrosine Kinase (BTK) Inhibitor Ibrutinib in Participants With Steroid Dependent/Refractory Chronic Graft Versus Host Disease (cGVHD)

PHASE3CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

May 1, 2018

Primary Completion Date

November 29, 2021

Study Completion Date

November 29, 2021

Conditions
Graft vs Host Disease
Interventions
DRUG

Ibrutinib

Participants will receive 420 mg (3 \* 140 mg capsules) oral ibrutinib once daily starting on Week 1 Day 1, unless they have intervening unacceptable toxicity or meet other criteria for participants discontinuation.

Trial Locations (15)

446-8602

Anjo Kosei Hospital, Anjo-shi

113 8677

Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Bunkyō City

730-8619

Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima

259-1193

Tokai University Hospital, Isehara

594-1101

Osaka Women's and Children's Hospital, Izumi

650 0047

Kobe City Medical Center General Hospital, Kobe

860-0008

National Hospital Organization Kumamoto Medical Center, Kumamoto

710-8602

Kurashiki Central Hospital, Kurashiki

371-0821

Gunmaken Saiseikai Maebashi Hospital, Maebashi

453-8511

Japanese Red Cross Nagoya Daiichi Hospital, Nagoya

663-8501

The Hospital of Hyogo College of Medicine, Nishinomiya

700 8558

Okayama University Hospital, Okayama

545 8586

Osaka City University Hospital, Osaka

060-8648

Hokkaido University Hospital, Sapporo

157 8535

National Center for Child Health and Development, Setagaya Ku

Sponsors
All Listed Sponsors
lead

Janssen Pharmaceutical K.K.

INDUSTRY