Blog

FDA Allows Pediatric Enrollment in Phase 1/2 Trial of FCX-007 Gene Therapy for RDEB – Epidermolysis Bullosa News

FDA Allows Pediatric Enrollment in Phase 1/2 Trial of FCX-007 Gene Therapy for RDEB
Epidermolysis Bullosa News
The U.S. Food and Drug Administration (FDA) will allow pediatric patients to enroll in the Phase 2 segment of an ongoing trial to evaluate FCX-007 as a potential gene therapy for recessive dystrophic epidermolysis bullosa (RDEB), Fibrocell Science

2018-02-01 NEWS
About Michael Zand

Leave a Reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.