November 13, 2008
Nymox Reports New Positive Results From Benign Prostatic Hyperplasia Study
Nymox Pharmaceutical, a biopharmaceutical company, has announced new positive results from the company's most recent study of NX-1207, its drug in development for benign prostatic hyperplasia.
A total of 67 patients and controls in this multi-center US study consisting of 92% of eligible patients were followed for an average of 59 weeks after a single administration of NX-1207. Of the patients given full dose NX-1207, 76.7% required no further treatment compared to 37.5% for controls (statistically significant, p=.012).
NX-1207 is a novel drug developed by Nymox which is in Phase III development for the treatment of BPH. The drug has successfully completed a series of blinded controlled multi-center US clinical trials where it has been found to produce improvements that are about double that reported for currently approved BPH drugs.
Paul Averback, CEO of Nymox, said: "We are extremely pleased with these new results, which are remarkably similar to the findings of a completely separate but comparable study reported in 2007. The consistent therapeutic response in a totally different trial in different subjects is very sound."