Nymox Pharmaceutical new updated Safety Committee review of safety data for its ongoing multi-center U.S. Phase 2 trial of NX-1207 has revealed no serious drug side effects. The entire cohort of enrolled subjects have now all completed their drug dosing in the trial. NX-1207 is Nymox's lead drug candidate for the treatment of benign
prostatic hyperplasia (BPH).
StreetInsider.com
Simplifying Global Compliance
Recommended Products
EU MDR Compliance: A Checklist for Meeting Manufacturing, Safety and Performance Requirements
The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing.
Accelerating Generic Drug Development: The FDA’s New Plan for Increasing Generic Competition
Accelerating Generic Drug Development explains the FDA’s new policy and shows how to navigate the new pathway to approval.
Editor's Picks
Indianapolis Firm Called Out for Complaint Investigations
The facility lacked adequate procedures for quality audits, the agency found.
Aquestive Petitions FDA to Halt Approval of NDA for Emergency Seizure Spray
Aquestive submitted a rolling NDA for its own seizure cluster drug in May.
FDAnews Drug Daily Bulletin
NYMOX PHARMACEUTICAL SAYS SAFETY COMMITTEE REVIEW ON PHASE 2 TRIAL OF NX-1207 REVEALS NO SERIOUS SIDE EFFECTS
June 28, 2006
