Head-to-head evidence

Belantamab mafodotin vs SENL103

Same mechanism, same race: design-graded trial evidence for both assets, with the grading rationale shown. Grades describe the quality of the evidence, never the merits of either security.

Multiple Myeloma

Shared mechanism: BCMA · full Multiple Myeloma pipeline

Belantamab mafodotin

Marketed by GlaxoSmithKline

Approved in Multiple Myelomaantibody-drug conjugate (anti-BCMA, MMAF payload)
Weak signal

NCT03525678 · Phase 2 · completed

This was a randomized but open-label phase 2 study in which all participants received belantamab mafodotin at one of two doses or formulations; there was no placebo or active comparator arm and no blinding. The primary endpoint was overall response rate by independent review, a clinical response measure, but the results are reported as per-arm rates with confidence intervals and no formal statistical comparison against a control, so the study cannot distinguish drug effect from natural history or placebo effect. The evidence is therefore descriptive phase 2 evidence of activity, not strong comparative evidence.

Next expected readout: October 2026 · NCT05573802 (registry estimate)

Unlock with Research ↗

SENL103

Developed by Hebei Senlang Biotechnology

Phase 1/2 in Multiple Myelomacell therapy (CAR-T)
Weak signal

NCT06067581 · Phase 1 · status unknown

This is a small, uncontrolled, open-label Phase 1 dose-escalation study with no comparator arm, designed to find a safe dose of SENL103 CAR-T therapy in heavily pretreated myeloma patients. Efficacy is only a secondary measure and no results have been posted, so there is no evidence yet of a clinical effect.

Next expected readout: February 2028 · NCT07421856 (registry estimate)

Unlock with Research ↗

The full competitive landscape for each asset (every same-race competitor with aligned evidence, sortable) is on the asset pages: Belantamab mafodotin's landscape · SENL103's landscape