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Epidermolysis Bullosa, Junctional

Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane.

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Phase 3 trials (1)

Phase 1 trials (2)

Organizations

Organization Involved with Phase 2 Indications (2)

Organization Involved with Phase 1 Indications (1)