drugset / Trial / NCT04998747

A Study of Subcutaneous (SC) AMG 701 in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)

NCT04998747

Phase 1 Withdrawn Amgen
Non-randomizedSequentialOpen-labelBasic science

Summary

A study to evaluate the safety and tolerability of subcutaneous (SC) AMG 701 in participants with relapsed or refractory multiple myeloma (RRMM) to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D)

Timeline

Start
2023-08-29
Primary completion
2025-08-02
Completion
2025-08-28

Drugs

EvaluationDrugModalityDoseRoute
Subject pavurutamab Protein / enzyme biologic Subcutaneous