Congenital Adrenal Hyperplasia

Posted 2 weeks ago by Wales Gene Park

Brief Summary: This is a Phase 3 study to evaluate the efficacy, safety, and tolerability of crinecerfont versus placebo administered for 24 weeks in approximately 165 adult subjects with classic CAH due to 21-hydroxylase deficiency. The study consists of a 6 month randomized, double blind, placebo-controlled period, followed by 1 year of treatment with crinecerfont. Duration of participation is approximately 20 months.

 Congenital Adrenal Hyperplasia /  Cardiff


No post found