Long-Term Follow-Up Study for Subjects Treated With P-BCMA-101

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

October 29, 2018

Primary Completion Date

August 31, 2032

Study Completion Date

November 30, 2032

Conditions
Multiple Myeloma
Interventions
DRUG

Rimiducid may be administered as indicated

Patients who received P-BCMA-101 in a previous trial will be evaluated in this trial for long term safety and efficacy. Rimiducid (safety switch activator) may be administered as indicated.

Trial Locations (13)

19104

University of Pennsylvania, Philadelphia

21201

University of Maryland Greenebaum Comprehensive Cancer Center, Baltimore

21205

Johns Hopkins University, Baltimore

37203

Sarah Cannon Research Institute at Tennessee Oncology, Nashville

Vanderbilt University Medical Center, Nashville

48201

Wayne State - Karmanos Cancer Institute, Detroit

60637

University of Chicago, Chicago

66205

University of Kansas Cancer Center, Westwood

77030

MD Anderson Cancer Center, Houston

80218

Colorado Blood Cancer Institute, Denver

92121

University of California, San Diego, San Diego

94143

University of California San Francisco, San Francisco

95618

University of California Davis, Davis

Sponsors
All Listed Sponsors
collaborator

California Institute for Regenerative Medicine (CIRM)

OTHER

lead

Poseida Therapeutics, Inc.

INDUSTRY

NCT03741127 - Long-Term Follow-Up Study for Subjects Treated With P-BCMA-101 | Biotech Hunter | Biotech Hunter