Suppression of Serum Luteinizing Hormone in Postmenopausal Women by an Orally Administered Nonpeptide Antagonist of the Gonadotropin-Releasing Hormone Receptor (NBI-42902)

• Published in: The journal of clinical endocrinology and metabolism 2006-10, Vol.91 (10), p.3903-3907
• Main Authors: Struthers, R. Scott, Chen, TaKung, Campbell, Bruce, Jimenez, Roland, Pan, Henry, Yen, Samuel S. C., Bozigian, Haig P.
• Format: Article
• Language: English
• Subjects: Administration, Oral; Aged; Biological and medical sciences; Double-Blind Method; Endocrinopathies; Female; Fundamental and applied biological sciences. Psychology; Humans; Luteinizing Hormone - antagonists & inhibitors; Luteinizing Hormone - blood; Medical sciences; Middle Aged; Postmenopause - blood; Thymine - analogs & derivatives; Thymine - pharmacokinetics; Thymine - pharmacology; Vertebrates: endocrinology
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/jc.2006-1110

Context: Parenteral administration of peptide GnRH analogs is widely used in clinical practice for the suppression of pituitary gonadotropins. NBI-42902 is an orally available, high-affinity nonpeptide antagonist of the human GnRH receptor. Objective: The objective was to evaluate the safety, pharmacokinetics, and inhibitory effects on gonadotropin secretion of NBI-42902 in postmenopausal women. Design: This was a phase I, double-blind, placebo-controlled, single-dose study with sequential dose escalation. Participants: Fifty-six healthy, postmenopausal women were included. FSH levels were greater than 40 IU/liter, and body mass index was within 20% of ideal values for all subjects. Interventions: Subjects were administered 5, 10, 25, 50, 75, 100, 150, or 200 mg NBI-42902 as an oral solution. Main Outcome Measures: Safety, tolerability, and serum LH and FSH concentrations were evaluated. Results: NBI-42902 was well tolerated. Serum LH concentrations rapidly declined, and dose-dependent suppression was observed. Maximal change from baseline LH concentrations ranged from −19 ± 5% in the 5-mg group to −55 ± 2% in the 150-mg group. Suppression of FSH was less pronounced (−15 to −22% of baseline). NBI-42902 was rapidly absorbed after oral administration with a terminal elimination half-life ranging from 2.7 ± 0.3 to 4.8 ± 0.8 h. A clear relationship between plasma NBI-42902 concentrations and LH suppression was evident. Conclusions: Dose-dependent LH suppression was achieved by oral administration of a nonpeptide GnRH antagonist suggesting that compounds such as NBI-42902 may enable adjustable gonadotropin suppression as part of novel treatment strategies for benign gynecological conditions.