A Study to Investigate the Safety and Efficacy of SAR446523 Injected Subcutaneously in Adult Participants With Relapsed/Refractory Myeloma

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

A FIRST-IN-HUMAN, OPEN-LABEL, PHASE 1 STUDY TO EVALUATE THE SAFETY, ANTITUMOR ACTIVITY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF SUBCUTANEOUS SAR446523, AN ANTI GPRC5D ADCC-ENHANCED MONOCLONAL ANTIBODY, IN PARTICIPANTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA

Intervention/treatment:
SAR446523
Medical condition:
RELAPSED OR REFRACTORY MULTIPLE MYELOMA
Protocol code:
TED18162
Control number:
289350
Status:
Recruiting
Approved:
September 11, 2024
Trial phase:
Phase 1
For more information:
ClinicalTrials.gov - NCT06630806
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Trial Transparency email recommended (Toll free for US & Canada)
Role
CONTACT
Phone:
800-633-1610
Extension option 6
Sponsor
SANOFI-AVENTIS CANADA INC

Locations

British Columbia

Investigational Site Number : 1240005
Vancouver, British Columbia, V5Z 1L3
RECRUITING

Quebec

Investigational Site Number : 1240001
Montreal, Quebec, H4A 3J1
RECRUITING
Investigational Site Number : 1240002
Sherbrooke, Quebec, J1H 5N4
RECRUITING
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