Washington Drug Letter
Oct. 15, 2012
| Vol.
44 No.
41
FDA Reclassifies Clinical Hold on Repros’ Mid-Stage Endometriosis Trial
The FDA reclassified its clinical hold on Repros Therapeutics’ Proellex and will now allow the company to conduct a Phase II trial of low-dose Proellex as a treatment for endometriosis.
This article is viewable by subscribers only. To view this article, please select an option below.
|