A Study of Ibrutinib in Combination With Rituximab, in Japanese Participants With Waldenstrom's Macroglobulinemia (WM)

PHASE2CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

September 25, 2019

Primary Completion Date

August 24, 2021

Study Completion Date

March 2, 2023

Conditions
Waldenstrom Macroglobulinemia
Interventions
DRUG

Ibrutinib

Ibrutinib 420 mg will be administered orally.

DRUG

Rituximab

Rituximab 375 mg/m\^2 will be administered intravenously.

Trial Locations (9)

296-8602

Kameda Medical Center, Chiba

104 0045

National Cancer Center Hospital, Chūōku

860 0008

National Hospital Organization Kumamoto Medical Center, Kumamoto

790-8524

Matsuyama Red Cross Hospital, Matsuyama

467 8602

Nagoya City University Hospital, Nagoya

545 8586

Osaka Metropolitan University Hospital, Osaka

565-0871

Osaka University Hospital, Suita

190-0014

National Hospital Organization Disaster Medical Center, Tachikawa

305 8576

University of Tsukuba Hospital, Tsukuba

Sponsors
All Listed Sponsors
lead

Janssen Pharmaceutical K.K.

INDUSTRY