HASBROUCK HEIGHTS, N.J.--(BUSINESS WIRE)--Nymox Pharmaceutical Corporation (NASDAQ: NYMX) announced today completion of a new long-term follow-up study of NX-1207 for benign prostatic hyperplasia (BPH). 114 subjects (representing 80% of eligible subjects) consented to participate in the blinded, placebo controlled study undertaken at clinical trial sites across the U.S. Individuals in the study were blindly assessed for symptomatic improvement, treatment outcomes, and durability of efficacy. Patients in the study were assessed 8 months to 19 months after NX-1207 or placebo treatment. The Company expects to complete statistical analysis of the data in the next 1-2 weeks and will be reporting the results once they are completed.
