Repros Receives FDA Guidance Regarding Clinical Program for Androxal

By: Benzinga
Repros Therapeutics (NASDAQ: RPRX ) today reported it has received guidance from the FDA regarding its clinical program for Androxal. The Company had previously submitted a list of questions with the final clinical study report for ZA-301. Repros subsequently provided an update of topline results from ZA-302 to the FDA. The
Data & News supplied by www.cloudquote.io
Stock quotes supplied by Barchart
Quotes delayed at least 20 minutes.
By accessing this page, you agree to the following
Privacy Policy and Terms and Conditions.