A PHASE I/II, OPEN-LABEL, MULTI-COHORT STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CEVOSTAMAB IN PRIOR B CELL MATURATION ANTIGEN-EXPOSED PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA
Primary Objective
This study will evaluate the efficacy, safety, and pharmacokinetics of cevostamab in participants with R/R MM. Sections 3.1 and 3.2 present the primary and secondary efficacy objectives for the study expressed using the estimand framework in accordance with the ICH E9(R1) statistical principles for clinical trials (FDA 2021b).
Details
Age
Adult
Type of Study
Treatment
Locations
CTRC Inpatient
University of Colorado Hospital
Principal Investigator
Daniel Sherbenou, MD, PhD
Study ID
Protocol Number: 22-0931
More information available at ClinicalTrials.gov: NCT05535244
Categories
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