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Medicus Pharma Reports Long-Acting Hormone Control in Phase 1 Teverelix Data

The results give the company a basis to begin endometriosis studies with a genetics-led design alongside Omics Labs.

Overview

  • Medicus said it will present company-reported results from two single-dose Phase 1 studies in 48 healthy premenopausal women at the AACE 2026 meeting.
  • The studies showed dose-dependent drops in estradiol, a key ovarian hormone, with some readings in the Barbieri range that aims to ease symptoms while limiting side effects.
  • Drug levels followed a depot-like pattern with rapid uptake, a later second peak, and a reported half-life of about 14 to 23 days that could allow fewer injections.
  • The company reported no unexpected safety issues and bone turnover markers stayed within normal ranges through Day 29 in these healthy volunteers.
  • Medicus plans patient trials for symptomatic endometriosis with Omics Labs in the UAE using biomarker-guided selection, highlighting a gap as no long-acting injectable GnRH antagonists are approved for this condition.