Oncolys BioPharma Inc. announced that it has received a notice from Transposon Therapeutics Inc., licensee of OBP-601 (censavudine, TPN-101), that enrollment has been completed with 42 patients randomized in the Phase IIa, double-blind, placebo- controlled study of OBP-601 in patients with Progressive Supranuclear Palsy (PSP). The target date for publication of the clinical trial results has not yet been determined. In addition, the Phase IIa, double-blind, placebo-controlled study in patients with Amyotrophic Lateral Sclerosis (ALS) and/or Frontotemporal Degeneration (FTD) is recruiting patients.
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- Oncolys BioPharma Inc. Announces Completion of Enrollment in Phase IIa Clinical Trial of OBP-601 (Censavudine, TPN-101) in Patients with Progressive Supranuclear Pals