MONTREAL--(BUSINESS WIRE)--GTx, Inc. (Nasdaq: GTXI) today presented a safety analysis demonstrating that fewer men treated with toremifene 80 mg had PSA progression over time compared to placebo in the Phase III clinical trial evaluating toremifene 80 mg for the treatment of multiple serious side effects of androgen deprivation therapy (ADT) for advanced prostate cancer. These data, as well as an additional analysis of bone turnover markers and fracture risk, were presented at the 2008 Annual Meeting of the American Society for Bone and Mineral Research in Montreal, Canada.
