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flag Clarity Pharmaceuticals' Phase III trial for a new prostate cancer imaging test has met its enrollment goal, showing strong demand and potential for FDA approval.

flag Clarity Pharmaceuticals has announced its Phase III AMPLIFY trial, evaluating Cu-SAR-bisPSMA PET/CT for detecting prostate cancer recurrence in men with rising PSA after treatment, has exceeded its target enrollment of about 220 participants across the U.S. and Australia. flag The non-randomized, single-arm study, which assesses imaging at 1–4 hours and 24 hours post-injection, is designed to support a U.S. FDA approval application. flag Rapid enrollment in nine months—despite existing PSMA PET options—signals strong clinical demand. flag Results will build on earlier trials showing improved detection over standard imaging. flag A second Phase III trial, CLARIFY, is ongoing and expected to conclude in 2026. flag To date, around 600 patients have been scanned globally, with over 350 in the past year.

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