NCT04910568: Phase 1b - Cevostamab in Participants With Relapsed or Refractory Multiple Myeloma

A Study Evaluating the Safety, Pharmacokinetics, and Activity of Cevostamab in Participants With Relapsed or Refractory Multiple Myeloma (CAMMA 1)

This Phase Ib, multicenter, open-label study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of cevostamab which will be administered to participants with relapsed or refractory multiple myeloma (R/R MM) via intravenous (IV) infusion using a modified weekly schedule.

Sponsor:

Genentech, Inc.

Collaborator:

Hoffmann-La Roche

Multiple locations

International Study

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ClinicalTrials.gov Identifier: NCT04910568

Official Title: An Open-Label, Multicenter, Phase Ib Trial Evaluating the Safety, Pharmacokinetics, and Activity of Cevostamab in Patients With Relapsed or Refractory Multiple Myeloma

First Posted : June 2, 2021

Click here for details on ClinicalTrials.gov

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Cevostamab

Cevostamab (Code C139549)

Anti-FCRH5 x Anti-CD3 Bi-specific T-cell Engager BFCR4350A

Anti-FCRH5/CD3 BiTE Antibody BFCR4350A

Anti-FCRH5/CD3 TDB BFCR4350A

BFCR4350A

Cevostamab

CEVOSTAMAB

FCRH5/CD3 T Cell Dependent Bispecific Antibody BFCR4350A

FCRH5/CD3 TDB Antibody BFCR4350A

Recombinant Anti-FCRH5 x Anti-CD3 Bi-specific T-cell Engager BFCR4350A

RO7187797

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- California: City of Hope Duarte

- Missouri: Washington University School of Medicine Saint Louis

- Colorado: Sarah Cannon/Colorado Blood Cancer Institute Denver

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Locations

United States, California

United States, Colorado

United States, Michigan

United States, Missouri

Australia, Victoria

Canada, Ontario