Sponsor:
Regeneron Pharmaceuticals
Code:
NCT07393282
Conditions
High Risk Smoldering Multiple Myeloma (HR-SMM)
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
Linvoseltamab
Daratumumab
Brief summary:
Conditions
High Risk Smoldering Multiple Myeloma (HR-SMM)
Study ID
NCT07393282
Start date
May 21, 2026
Status verified date
Oct, 2026
Completion date
Jul 27, 2033
Anticipated
Primary completion date
Jul 27, 2033
Anticipated
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Enrollment
270 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
experimental: Linvoseltamab
active comparator: Daratumumab
Interventions
Linvoseltamab
Daratumumab
Primary outcome measure
Central contacts
Locations
Mayo Clinic Phoenix, Mayo Clinic Building
Recruiting
Phoenix, Arizona, United States, 85054
Emory University - Winship Cancer Institute
Recruiting
Atlanta, Georgia, United States, 30322
Dana Farber / Harvard Cancer Center
Recruiting
Boston, Massachusetts, United States, 02215
Barbara Ann Karmanos Cancer Institute - Detroit
Recruiting
Detroit, Michigan, United States, 48201
Mayo Clinic
Recruiting
Rochester, Minnesota, United States, 55905
Washington University School of Medicine in St. Louis
Recruiting
St Louis, Missouri, United States, 63110
Memorial Sloan Kettering Cancer Center
Recruiting
New York, New York, United States, 10021
Columbia University Medical Center
Recruiting
New York, New York, United States, 10032
Ohio State University
Recruiting
Columbus, Ohio, United States, 43210
Sponsor
Regeneron Pharmaceuticals
Last update posted
Oct 21, 2026
Last verified
Oct, 2026
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-23. This information was provided to ClinicalTrials.gov by Regeneron Pharmaceuticals on 2026-10-21. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.