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NCT04484623: Phase 3 - Belantamab Mafodotin & Pom/Dex (Pd) Vs Bortezomib & Pd in Ref. MM (DREAMM 8)

Updated: Sep 19, 2022

DREAMM 8

Relapsed & Refractory Myeloma

DREAMM 8 belantamab myeloma study

Belantamab Mafodotin Plus Pomalidomide and Dexamethasone (Pd) Versus Bortezomib Plus Pd in Relapsed/Refractory Multiple Myeloma (DREAMM 8)


This study will evaluate the efficacy and safety of belantamab mafodotin in combination with pomalidomide and dexamethasone (Arm A) compared with that of combination of pomalidomide, bortezomib and dexamethasone (Arm B) in participants with relapsed/refractory multiple myeloma (RRMM).


Sponsor

 

ClinicalTrials.gov Identifier: NCT04484623

Official Title: A Phase III, Multicenter, Open-Label, Randomized Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination With Pomalidomide and Dexamethasone (B-Pd) Versus Pomalidomide Plus Bortezomib and Dexamethasone (PVd) in Participants With Relapsed/Refractory Multiple Myeloma (DREAMM 8)

First Posted : July 23, 2020

Click here to see details on ClinicalTrials.gov


 



 

Belantamab Mafodotin

GSK2857916


Drug: Belantamab mafodotin

Drug: Pomalidomide

Drug: Dexamethasone

Drug: Bortezomib

 

Locations

United States, Arizona

United States, Colorado

United States, Florida

United States, Massachusetts

United States, Missouri

United States, Pennsylvania

United States, Tennessee

United States, Washington

United States, Wisconsin

Canada

Canada, Ontario

Australia, Australian Capital Territory

Australia, New South Wales

Australia, Queensland

Australia, South Australia

Australia, Victoria

Australia, Western Australia

New Zealand

Europe

United Kingdom

France

Germany

Italy

Spain

Czechia

Greece

Poland

Turkey

Asia

Israel

Japan

Korea, Republic of

Russian Federation

 

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