Fda approves Zevaskyn for rare, genetic skin disorder

The U.S. Food and Drug Administration has approved Abeona Therapeutics’ Zevaskyn (prademagene zamikeracel) for patients with the rare, genetic skin disorder recessive dystrophic epidermolysis bullosa.

This article was originally published on MedicalXpress.com

You may also be interested in:

Read More:

Lawyers Lookup