Latest News and Press Releases
Want to stay updated on the latest news?
-
Full response to November meeting submitted to FDA Repros believes all FDA questions positively addressed Company expects contract organization to officially submit NDA to FDA...
-
Low dose oral Proellex® study in women with fibroids and heavy menstrual bleeding initiated Vaginal administration of Proellex® in women with fibroids and heavy menstrual bleeding...
-
THE WOODLANDS, Texas, Dec. 29, 2014 (GLOBE NEWSWIRE) -- Repros Therapeutics Inc.® (Nasdaq:RPRX) today announced a federal judge in Texas has issued a definitive ruling finding correct...
-
THE WOODLANDS, Texas, Nov. 10, 2014 (GLOBE NEWSWIRE) -- Repros Therapeutics Inc.® (Nasdaq:RPRX) today announced financial results for the third quarter ended September 30, 2014. Financial...
-
No New Clinical Studies Requested Environmental Impact Assessment Plan Will be Discussed With FDA Prior to NDA Submission Company to Host Conference Call on Friday, November 7,...
-
THE WOODLANDS, Texas, Oct. 27, 2014 (GLOBE NEWSWIRE) -- Repros Therapeutics Inc.® (Nasdaq:RPRX) today announced that it will host a live webcast of its Investor and Analyst Day that is being held...
-
No evidence of negative effects on bone mineral density Treatment benefit is sustained with 79.3% of subjects exhibiting normal morning testosterone after 12 months of treatment (LOCF...
-
THE WOODLANDS, Texas, Oct. 16, 2014 (GLOBE NEWSWIRE) -- Repros Therapeutics Inc.® (Nasdaq:RPRX) today reported that its upcoming meeting with the FDA in the first half of November will be a Type...
-
THE WOODLANDS, Texas, Sept. 26, 2014 (GLOBE NEWSWIRE) -- Repros Therapeutics Inc.® (Nasdaq:RPRX) today reported it has been granted a Type B Pre-NDA meeting with the FDA in the first half of...
-
44.2% of Topical T subjects below 10 million sperm/mL at end of study versus 2.4% and 0.0% respectively for Androxal® and placebo ITT (Androxal® vs. Topical T, p < 0.0001) 71.5%...