The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: A Study of JNJ-64407564 in Japanese Participants With Relapsed or Refractory Multiple Myeloma
Official Title: A Phase 1 Study of JNJ-64407564, a Humanized GPRC5D * CD3 Bispecific Antibody in Japanese Subjects With Relapsed or Refractory Multiple Myeloma
Study ID: NCT04773522
Brief Summary: The purpose of this study is to evaluate the safety and tolerability in Japanese participants with relapsed or refractory multiple myeloma (MM) at the recommended Phase 2 dose (RP2D) identified in NCT03399799 study.
Detailed Description:
Minimum Age: 20 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Shonan Kamakura General Hospital, Kamakura-shi, , Japan
National Cancer Center Hospital East, Kashiwa, , Japan
Nagoya City University Hospital, Nagoya, , Japan
National Hospital Organization Okayama Medical Center, Okayama, , Japan
Japanese Red Cross Medical Center, Shibuya, , Japan
Iwate Medical University Hospital, Shiwa-gun, , Japan
Name: Janssen Pharmaceutical K.K., Japan Clinical Trial
Affiliation: Janssen Pharmaceutical K.K.
Role: STUDY_DIRECTOR