OncologyFDA Approved

Relugolix (Orgovyx)

Oral

Overview

Relugolix is an orally bioavailable non-peptide gonadotropin-releasing hormone (GnRH) receptor antagonist. Although it is not a peptide, it exerts its therapeutic effect through the same mechanism as peptide GnRH antagonists, competitively blocking pituitary GnRH receptors to suppress gonadotropin and sex steroid production.

Mechanism of Action

It is indicated for advanced prostate cancer and, in combination formulation, for management of heavy menstrual bleeding associated with uterine fibroids and moderate to severe endometriosis pain. The oral route of administration offers a distinct advantage over depot peptide formulations..

Research Summary & Key Findings

Relugolix received FDA approval in 2020 for advanced prostate cancer based on the HERO trial (NEJM 2020), which demonstrated sustained castration in 96.7% of patients compared to 88.8% on leuprolide, with a significantly lower risk of major adverse cardiovascular events. In 2021, a combination product (relugolix with estradiol and norethindrone) was approved for uterine fibroids based on phase 3 trials showing reduction in menstrual blood loss. The rapid reversibility of suppression upon discontinuation is a distinguishing pharmacological feature.

Clinical Status

FDA Approved

Relugolix (Orgovyx) has received FDA approval and is available for clinical use under appropriate medical supervision. Consult a qualified healthcare provider for prescribing information.

Administration Routes

Oral

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Disclaimer: This information is provided for educational and research purposes only. It is not intended as medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before starting any peptide therapy. The Peptide Association does not endorse or recommend any specific treatment protocol.