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Medicus Pharma gets FDA feedback and IRB approval for streamlined Phase 2 study of Teverelix in acute urinary retention.

Market News
16 Jul 2026
GlobeNewsWire
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Bullish
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Medicus Pharma announced positive FDA feedback and central IRB approval for its optimized Phase 2 study of Teverelix, a long-acting GnRH antagonist, targeting men after a first episode of acute urinary retention (AUR). The redesigned study will enroll about 126 patients, down from the previously planned 390, aiming to generate early pharmacodynamic data and support dose and route optimization. FDA recommendations are operational and do not affect the study's scientific goals. This streamlined approach is expected to accelerate development, optimize capital use, and provide robust data to guide future regulatory and clinical decisions.

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