A Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination With Standard of Care in Participants With Relapsed-Refractory Multiple Myeloma (RRMM)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorGlaxoSmithKline

About this trial

This study is for adults with multiple myeloma (a type of blood cancer) that has come back after being treated earlier or isn't responding to the current treatment.

The main goal is to find out if the study drug, belantamab mafodotin, given less often (on an extended schedule) with other cancer medicines, can still treat the cancer effectively while causing fewer side effects, especially those affecting the eyes. The study will also look at how well the treatment works overall and how safe it is when administered to the participants.

Eligibility criteria

Qualifiers

Male or female, 18 years or older (at the time consent is obtained).

Have a confirmed diagnosis of Multiple Myeloma (MM) as defined by the International Myeloma Working Group (IMWG) criteria.

Eastern Cooperative Oncology Group (ECOG) performance status of zero to 2.

Have been previously treated with at least 1, but no more than 2, prior lines of MM therapy and must have documented disease progression during or after their most recent therapy.

Disqualifiers

Active plasma cell leukemia at Screening.

Symptomatic amyloidosis, including active Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal plasma proliferative disorder, and Skin changes (POEMS).

The disease must be considered medically stable for at least 2 years; or

The patient must not be receiving active therapy, other than hormonal therapy for this disease.

Trial design

Treatments tested in this trial

  • Belantamab mafodotin
  • Dexamethasone
  • Pomalidomide
  • Bortezomib
  • Carfilzomib

Treatment groups

200 Participants
are divided into 3 treatment groups

Sponsors and collaborators