Reata gets FDA OK for Friedreich’s Ataxia treatment

FRIEDREICH’S ATAXIA IS AN ULTRA-RARE, PROGRESSIVE, NEUROMUSCULAR DISEASE THAT AFFECTS APPROXIMATELY 5,000 DIAGNOSED PATIENTS IN THE UNITED STATES

SKYCLARYS IS INDICATED FOR THE TREATMENT OF FRIEDREICH’S ATAXIA IN ADULTS AND ADOLESCENTS AGED 16 YEARS AND OLDER

RARE PEDIATRIC DISEASE PRIORITY REVIEW VOUCHER GRANTED

MANAGEMENT TO HOST CONFERENCE CALL TODAY, FEBRUARY 28, 2023, AT 6:00 PM ET

Reata Pharmaceuticals, Inc. (Nasdaq: RETA) ("Reata," the "Company," "our," "us," or "we"), a biopharmaceutical company focused on developing and commercializing novel therapies for patients with severe diseases, announced that the U.S. Food and Drug Administration ("FDA") has approved SKYCLARYS™ (omaveloxolone) for the treatment of Friedreich’s ataxia in adults and adolescents aged 16 years and older. With this approval, the FDA granted a rare pediatric disease priority review voucher.

Reata’s management will host a conference call on February 28, 2023, at 6:00 pm ET. The conference call will be accessible by dialing (844) 200-6205 (toll-free domestic) or (929) 526-1599 (international) using access code 827526. The webcast link is https://events.q4inc.com/attendee/939887927.

https://finance.yahoo.com/news/reata-pharmaceuticals-announces-fda-approval-222500644.html