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BLENREP belantamab mafodotin

Study overview

Study design

A head-to-head trial designed to study the efficacy of a BLENREP triplet (BVd) vs a daratumumab triplet (DVd) in RRMM

DREAMM-7: A Phase 3, open-label, randomized multicentre study with MM patients who received at least one prior therapy.

DREAMM-7 study design schematic showing BVd versus DVd arms, randomization, and treatment cycles.
Adapted from the Product Monograph.

A pivotal Phase 3 trial designed to study the efficacy of a BLENREP triplet (BPd) vs a pomalidomide triplet (PVd) in RRMM

DREAMM-8: A Phase 3, open-label, randomized multicentre study with MM patients who received at least one prior therapy including lenalidomide.

DREAMM-8 study design schematic showing BPd versus PVd arms, randomization, and treatment cycles.
Adapted from the Product Monograph.

Baseline characteristics

DREAMM-7: baseline characteristics were balanced in both arms

DREAMM-7 baseline characteristics table comparing BVd and DVd arms.
Adapted from the Product Monograph.

DREAMM-8: baseline characteristics were balanced in both arms

DREAMM-8 baseline characteristics table comparing BPd and PVd arms.
Adapted from the Product Monograph.

Eligibility criteria

Both DREAMM-7 and DREAMM-8 used the same key eligibility and exclusion criteria.

Key eligibility criteria1:

  • A confirmed diagnosis of MM as defined by International Myeloma Working Group (IMWG) criteria
  • Previous treatment with at least 1 line of MM therapy
  • Documented disease progression during or after their most recent therapy
  • ECOG status of 0–2

Key exclusion criteria1:

  • Patients refractory or intolerant to daratumumab or bortezomib, or with prior exposure to anti-BCMA therapy
  • Patients with current corneal disease (except for mild punctate keratopathy)

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References

  1. BLENREP Product Monograph. GSK, [Date placeholder].
  2. Hungria V, et al. N Engl J Med. 2025;392(13):1213–1224. (DREAMM-7)
  3. Trudel S, et al. N Engl J Med. 2025;393(2):166–178. (DREAMM-8)