Mucous membrane pemphigoid

MONDO:0018746

Mucous membrane pemphigoid is a bullous dermatosis characterized clinically by blistering of the mucous membranes followed by scarring, and immunologically by IgG, IgA and/or C3 deposits on the epidermal basement membrane.

Also known as: Mucosynechial pemphigoid, benign mucous Membrane pemphigoid, cicatricial pemphigoid, mucosal pemphigoid, benign mucosal pemphigoid, benign mucous membrane pemphigoid, benign mucous membrane pemphigoid with ocular involvement, cicatricial pemphigoid with ocular involvement

46 clinical trials for this condition and its sub-types, 5 tagged with Mucous membrane pemphigoid itself.

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Where it sits in the disease tree

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Part of

↑ Autoimmune bullous skin disease (56)

Sub-types of Mucous membrane pemphigoid

Ocular cicatricial pemphigoid 4 trials

Including sub-types (46) Tagged with Mucous membrane pemphigoid (5)

Trials to join now! 4 Not yet finished but already full! 1

New hope for rare blistering disease: rituximab vs standard therapy

Disease control Ongoing

This study compares two drugs, rituximab and cyclophosphamide, in 92 adults with severe mucous membrane pemphigoid, a rare autoimmune disease that causes painful blisters and scarring on mucous membranes. The goal is to see which treatment is safer and more effective at controlli…

Phase 3 • Sponsor: University Hospital, Rouen • Aim: Disease control

Last updated Jun 27, 2026 13:05 UTC

Mucous membrane pemphigoid

Where it sits in the disease tree

New hope for rare blistering disease: rituximab vs standard therapy