drugset / Trial / NCT07030517

A Study to Assess Safety of Teclistamab in Indian Participants With Relapsed and Refractory Multiple Myeloma

NCT07030517

Phase 4 Recruiting 75 enrolled Johnson & Johnson Private Limited
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety of teclistamab in routine clinical practice when given as monotherapy in Indian participants with relapsed and refractory multiple myeloma (RRMM) (that is, a blood cancer that comes back after treatment or does not respond to treatment) who have previously received at least 3 prior lines of therapy including an immunomodulatory agent, a proteasome inhibitor and an anti-cluster of differentiation (CD)38 antibody (is a protein that fights infection) and whose disease have progressed on the last therapy.

Timeline

Start
2025-05-22
Primary completion
2026-11-03
Completion
2027-06-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Teclistamab Monoclonal antibody Subcutaneous

Indications