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
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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