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NCT07150091

Sub-study of Belantamab Mafodotin (GSK2857916) in Combination With Nirogacestat, Lenalidomide, and Dexamethasone in Participants With RRMM

Active, enrolled Phase 1, PHASE2 Last updated 2 September 2025
What this trial tests

Phase 1, PHASE2 trial testing Belantamab mafodotin in Multiple Myeloma in 20 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
19 July 2022
Primary endpoint
17 April 2025
11 March 2027

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 1, PHASE2
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date19 July 2022
Primary completion17 April 2025
Estimated completion11 March 2027
Sites12 locations across France, Greece, Germany, Mexico, South Korea, Canada, United States, Brazil

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

18 and older, any sex, with Multiple Myeloma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary purpose is to determine the safety and tolerability of belantamab mafodotin in combination with nirogacestat, lenalidomide, and dexamethasone, and to establish the recommended Phase 2 dose for combination treatment to explore in the cohort expansion (CE) phase in participants with RRMM. This study is a sub study of the Master protocol (NCT04126200).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Belantamab mafodotin

Trials testing the same drug.

Other recruiting trials for Multiple Myeloma

Currently open trials in the same condition.

Other GlaxoSmithKline trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07150091.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing