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Orgovyx

relugolix
GnRH Receptor Antagonist (Oral) Myovant Sciences FDA Approved 2020
Indications Dosing Forms Contraindications Warnings Adverse Reactions Pharmacology Clinical Studies Tumor Types
1. Indications and Usage

Advanced prostate cancer.

2. Dosage and Administration

Loading dose: 360 mg (three 120 mg tablets) orally on Day 1
Maintenance: 120 mg orally once daily
Take with or without food
Missed dose >24 hours: Testosterone may recover; consider re-loading

3. Dosage Forms and Strengths

Tablets: 120 mg

4. Contraindications

None listed.

5. Warnings and Precautions
  • QT/QTc Prolongation: Androgen deprivation therapy may prolong QTc. Consider risks vs benefits in patients with pre-existing QTc prolongation or risk factors.
  • Cardiovascular Disease: ADT increases risk of MI, sudden cardiac death, and stroke. HERO trial showed lower major adverse cardiovascular events (MACE) vs leuprolide (2.9% vs 6.2%).
  • Loss of Bone Mineral Density: Long-term ADT increases fracture risk. Consider DEXA scan.
  • Hyperglycemia and Diabetes: Monitor blood glucose.
  • Embryo-Fetal Toxicity
6. Adverse Reactions
Most Common Adverse Reactions

Hot flush (54%), musculoskeletal pain (30%), fatigue (26%), constipation (12%), diarrhea (12%), arthralgia (12%), decreased libido (5%), weight gain (3%)

Hot flush
54%
Musculoskeletal Pain
30%
Fatigue
26%
Constipation
12%
Diarrhea
12%
Arthralgia
12%
Decreased Libido
5%
Weight Gain
3%

Consult the complete prescribing information for a comprehensive list of adverse reactions and their frequencies.

12. Clinical Pharmacology
Mechanism of Action

Relugolix is a non-peptide, oral gonadotropin-releasing hormone (GnRH) receptor antagonist. It competitively binds to GnRH receptors in the anterior pituitary, directly blocking GnRH signaling without the initial stimulatory phase (testosterone surge/flare) seen with GnRH agonists (leuprolide, goserelin). This results in rapid suppression of LH, FSH, and consequently testosterone to castrate levels (typically within 4 days). Unlike injectable GnRH agonists, testosterone recovery upon discontinuation is faster (~90 days), and there is no flare phenomenon.

Pharmacokinetics

Tmax: 2-4 hours. Half-life: approximately 25 hours. Protein binding: 68-71%. Metabolized by CYP3A and P-gp (as substrate). Steady-state by Day 7. Excreted in feces (81%) and urine (4.1%). High-fat meals reduce Cmax by 28%.

14. Clinical Studies

Clinical efficacy and safety data supporting the approval are available in the full prescribing information and from the clinical trials listed below.

Pivotal Clinical Trials
Additional Resources
Approved Tumor Types