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Nymox’s lead candidate, Fexapotide Triflutate (FT), has completed Phase 3 clinical trials in over 1,700 patients across more than 70 U.S. centers for benign prostatic hyperplasia. The company plans to file for regulatory approval in major markets including the U.S. and Europe. FT has also shown long-term benefits in a Phase 2 trial for early-stage prostate cancer with significant delay of disease progression compared to controls. The company also markets diagnostic tests NicAlert® and TobacAlert®.
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