DREAMM 7: A Multicenter, Open-Label, Randomized Phase III Study to Evaluate the Efficacy and Safety of the Combination of Belantamab Mafodotin, Bortezomib, and Dexamethasone (B-Vd) Compared With the Combination of Daratumumab, Bortezomib and Dexamethasone (D-Vd) in Participants With Relapsed/Refractory Multiple Myeloma
Latest Information Update: 26 May 2025
At a glance
- Drugs Belantamab mafodotin (Primary) ; Bortezomib; Daratumumab; Dexamethasone; Dexamethasone
- Indications Multiple myeloma
- Focus Registrational; Therapeutic Use
- Acronyms DREAMM-7
- Sponsors GlaxoSmithKline; GlaxoSmithKline Research & Development; GSK
Most Recent Events
- 19 May 2025 According to a GSK media release, based on positive results from the DREAMM-7 and DREAMM-8 phase III trials, company announced approval of Blenrep combinations by Japan's Ministry of Health, Labour and Welfare (MHLW) for the treatment of adults with relapsed or refractory multiple myeloma.
- 09 Dec 2024 According to a GSK media release, based on DREAMM-7 and DREAMM-8 results, a new drug application (NDA) for Blenrep (belantamab mafodotin) in combinations with bortezomib plus dexamethasone (BorDex [BVd]) and pomalidomide plus dexamethasone (PomDex [BPd]) for the treatment of patients with multiple myeloma who have received at least one prior line of therapy has been accepted in Japan (with priority review), United Kingdom, Canada and Switzerland (with priority review for DREAMM-8).
- 09 Dec 2024 According to a GSK media release, based on results from this trial, the National Medical Products Administration (NMPA) of China has accepted for review a new drug application (NDA) for Blenrep (belantamab mafodotin) in combination with bortezomib plus dexamethasone (BVd) as a treatment for relapsed or refractory multiple myeloma.