Head-to-head evidence

Depemokimab vs Mepolizumab

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.

Chronic Obstructive Pulmonary Disease

Shared mechanism: IL-5 · full Chronic Obstructive Pulmonary Disease pipeline

Depemokimab

Marketed by GlaxoSmithKline

Phase 3 in Chronic Obstructive Pulmonary Diseasemonoclonal antibody
not yet graded

No graded featured trial for this indication yet; the grade above reflects that absence, not a judgment.

Next expected readout: April 2029 · NCT07177339 (registry estimate)

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Mepolizumab · Nucala

Marketed by GlaxoSmithKline

Approved in Chronic Obstructive Pulmonary Diseasemonoclonal antibody
Partial signal

NCT01463644 · Phase 3 · completed

Participants were randomly assigned and quadruple-blinded to mepolizumab or placebo, but only 18 people were enrolled. The primary endpoint was a sputum eosinophil biomarker rather than a clinical outcome, and the registry does not state whether the between-group difference was statistically significant, so the result is unclear.

Next expected readout: February 2028 · NCT07749001 (registry estimate)

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Asthma

Shared mechanism: IL-5 · full Asthma pipeline

Depemokimab

Marketed by GlaxoSmithKline

Approved in Asthmamonoclonal antibody
Partial signal

NCT04718389 · Phase 3 · completed

This was a large randomized, double-blind, active-controlled trial comparing depemokimab with mepolizumab or benralizumab, using the clinically meaningful primary endpoint of annualized clinically significant asthma exacerbations. The primary results were 0.57 versus 0.49 exacerbations per participant-year (rate ratio 1.16, 95% CI 0.98–1.38; p=0.079), but the record does not provide the non-inferiority margin, so it is not possible to confirm that the primary endpoint was met.

Next expected readout: February 2027 · NCT07828327 (registry estimate)

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Mepolizumab · Nucala

Marketed by GlaxoSmithKline

Approved in Asthmamonoclonal antibody
Partial signal

NCT01691859 · Phase 3 · completed

This was an open-label, single-arm long-term extension of the prior MEA112997 trial, enrolling 347 participants who had received at least two doses in that study. Because there was no randomization, blinding, or control group, the primary safety endpoint was descriptive rather than a comparative efficacy test, although the explicit extension design provides follow-up evidence beyond the original randomized trial.

Next expected readout: October 2026 · NCT07343661 (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: Depemokimab's landscape · Mepolizumab's landscape