Medicus Pharma Ltd. to Present Promising Data on Teverelix at AACE Annual Meeting 2026
PHILADELPHIA, Jan. 12, 2026 (GLOBE NEWSWIRE) — Medicus Pharma Ltd. (NASDAQ: MDCX), a precision-guided biotech company, is set to present significant findings on its product, Teverelix, at the American Association of Clinical Endocrinology (AACE) Annual Meeting, scheduled for April 22–24, 2026, in Las Vegas, Nevada. This presentation will shed light on the long-acting gonadotropin-releasing hormone (GnRH) antagonist's effects on bone turnover in healthy female volunteers.
Clinical Findings from Phase 1 Studies
The abstract titled "Evaluation of Teverelix, a Long-Acting GnRH Antagonist: Pharmacokinetics, Pharmacodynamics, Bone Turnover and Safety in Two Phase 1 Studies in Healthy Female Volunteers" contains results derived from two randomized, placebo-controlled Phase I clinical studies involving 48 premenopausal women.
These studies aimed to assess:
- Absorption rates of Teverelix
- Suppression of reproductive hormones
- Effects on bone turnover markers
- Overall safety following single subcutaneous injections
Key Highlights of Teverelix's Phase 1 Results
The findings from both studies yielded several noteworthy results:
- Rapid suppression of LH and FSH within 24 hours of dosing.
- Reversible estradiol suppression, with numerous participants achieving levels between 30–50 pg/mL, mitigating bone loss risks.
- Sustained hormone suppression lasting up to two to three weeks post-injection at higher dosages.
- Stable bone turnover markers indicating no short-term evidence of bone loss.
- A favorable safety profile, with no serious drug-related adverse events.
Expert Insights on Teverelix
Dr. Raza Bokhari, Executive Chairman and CEO of Medicus, remarked: “We believe that these findings reinforce the versatility of Teverelix as a long-acting GnRH antagonist platform. The results support its advancement in treating women’s health conditions such as endometriosis, affecting approximately 10% of women of reproductive age worldwide.”
He added, “We are currently planning a Phase 2 genomics-informed study of Teverelix in women with symptomatic endometriosis, scheduled to take place in the United Arab Emirates (UAE).”
Understanding Teverelix's Mechanism
Teverelix trifluoroacetate is an innovative long-acting injectable GnRH antagonist designed to offer immediate suppression of LH, FSH, and downstream sex hormones without causing an initial hormonal surge. This mechanism is particularly relevant for patients with advanced prostate cancer who are at heightened cardiovascular risk.
Strategic Development and Future Plans
Medicus Pharma Ltd. is focused on advancing select programs through Phase 2 proof-of-concept studies while seeking strategic partnerships for late-stage development and commercialization. The ongoing efforts include:
- Completing decision-grade clinical and regulatory data packages.
- Advancing the SkinJect™ Program for the treatment of basal cell carcinoma (BCC).
In addition to Teverelix, the company expects to share topline data from SkinJect™ in Q1 2026.
About Medicus Pharma Ltd.
Medicus Pharma Ltd. (Nasdaq: MDCX) is dedicated to accelerating the clinical development of novel therapeutics and is involved in projects across multiple countries. Its subsidiary, SkinJect Inc., focuses on non-invasive treatments for basal cell skin cancer using innovative microneedle technology.