Head-to-head evidence

MB12 vs Retifanlimab

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.

Non-Small Cell Lung Cancer

Shared mechanism: PD-1 · full Non-Small Cell Lung Cancer pipeline

MB12

Developed by Laboratorio Elea Phoenix S.A.

Phase 3 in Non-Small Cell Lung Cancermonoclonal antibody
Partial signal

NCT05668650 · Phase 3 · status unknown

This is a randomized, double-blind, active-controlled trial with over 170 patients, but its primary comparison is a pharmacokinetic equivalence check between MB12 and the reference drug rather than a clinical efficacy comparison. No results have been posted yet.

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Retifanlimab

Marketed by Incyte

Phase 3 in Non-Small Cell Lung Cancermonoclonal antibody
Reliable signal

NCT04205812 · Phase 3 · completed

Participants were randomly assigned and double-blinded to receive retifanlimab or placebo with standard chemotherapy, with 391 in the retifanlimab group and 192 in the control group. The hard clinical primary endpoint of overall survival was met, favoring retifanlimab (hazard ratio 0.75; p=0.0042).

Next expected readout: December 2027 · NCT07219576 (registry estimate)

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The full competitive landscape for each asset (every same-race competitor with aligned evidence, sortable) is on the asset pages: MB12's landscape · Retifanlimab's landscape