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A Phase II, Multicentre, Double-blind, Placebo Controlled, Pilot Study to Evaluate the Safety and Efficacy of CUV1647 Administered as A Subcutaneous Bioresorbable 16mg Implant in Patients Undergoing Photodynamic Therapy (PDT) utilising Porfimer Sodium Results

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This phase 3 global registration study involved 2,539 participants and met its primary endpoints for both mean percent change in body weight and the percentage of participants achieving 5% body weight reductions