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Jul 14, 2026Trial update

Abeona registers long-term safety registry for ZEVASKYN gene therapy in RDEB

Abeona Therapeutics has registered an observational post-marketing study tracking patients treated with prademagene zamikeracel for recessive dystrophic epidermolysis bullosa.

Abeona Therapeutics posted one new registry study during the week covering its approved RDEB gene therapy.

  • Abeona registered a post-marketing observational registry (NCT07700966) for patients treated with prademagene zamikeracel, also known as ZEVASKYN or pz-cel, for recessive dystrophic epidermolysis bullosa. The study is designed to evaluate long-term safety and wound healing durability for up to 15 years in treated participants1, with an estimated enrollment of 250 participants across 4 U.S. sites, and status listed as recruiting.

Written by readthrough’s AI from the linked primary sources and fact-checked against them automatically before publishing. Not investment advice.