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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.
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.
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.
Rapid enrollment in nine months—despite existing PSMA PET options—signals strong clinical demand.
Results will build on earlier trials showing improved detection over standard imaging.
A second Phase III trial, CLARIFY, is ongoing and expected to conclude in 2026.
To date, around 600 patients have been scanned globally, with over 350 in the past year.
El ensayo de Fase III de Clarity Pharmaceuticals para una nueva prueba de diagnóstico por imágenes del cáncer de próstata ha alcanzado su objetivo de inscripción, mostrando una fuerte demanda y potencial para la aprobación de la FDA.