Medicus Pharma Ltd. Common StockUAE DOH authorization for Phase 2a trial is a regulatory approval advancing the drug's development.

Medicus Pharma Ltd. has received Investigational New Drug authorization from the Department of Health – Abu Dhabi for its Phase 2a PRECISION-E2 trial of Teverelix in women with symptomatic endometriosis in the United Arab Emirates. The randomized, placebo-controlled study will enroll approximately 84 participants and evaluate three treatment regimens: 60 mg and 90 mg administered subcutaneously, and 90 mg intramuscularly. The primary goal is to identify the proportion of participants achieving and maintaining serum estradiol levels within the Barbieri therapeutic window of approximately 20 to 50 picograms per milliliter for at least 14 consecutive days. Teverelix, a gonadotrophin-releasing hormone antagonist developed by subsidiary Antev Ltd., is designed to suppress reproductive hormones without an initial hormonal flare. The authorization follows review of chemistry, manufacturing and controls, non-clinical, clinical, and safety documentation, with the study still subject to site-specific Institutional Review Board and ethics approvals.
Medicus Pharma Ltd. Common StockUAE DOH authorization for Phase 2a trial is a regulatory approval advancing the drug's development.
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