First-in-Human, Double-Blind, Randomized Controlled Trial of an Oral Dose of GnRH Antagonist TU2670 in Healthy Women.

Autor:	Sungpil Han, Yong-Soon Cho, Seok-Kyu Yoon, Kyoung Soo Lim, Sang-Heon Cho, JaeWoo Kim, Sangmin Choe, Jinah Jung, Jong-Lyul Ghim, SangKeun Choi, Minhee Lee, Seon Mi Kim, Hun-Taek Kim, Hyeong-Seok Lim, Jae Yoon Shim, Kyun-Seop Bae, Han, Sungpil, Cho, Yong-Soon, Yoon, Seok-Kyu, Lim, Kyoung Soo
Předmět:	LUTEINIZING hormone releasing hormone MENSTRUAL cycle SEX hormones INFERTILITY HEPATITIS associated antigen PERIMENOPAUSE RESEARCH HORMONE antagonists FOLLICLE-stimulating hormone HUMAN research subjects ORAL drug administration ESTRADIOL RESEARCH methodology MEDICAL cooperation EVALUATION research COMPARATIVE studies RANDOMIZED controlled trials LUTEINIZING hormone BLIND experiment DOSE-effect relationship in pharmacology OVULATION
Zdroj:	Journal of Clinical Endocrinology & Metabolism; Mar2021, Vol. 106 Issue 3, pe1111-e1120, 10p
Abstrakt:	Objective: To evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of TU2670, a novel orally active, nonpeptide gonadotropin-releasing hormone (GnRH) antagonist administered to healthy female participants.Methods: This was a first-in-human, multicenter, phase 1, randomized, double-blind, placebo-controlled, single-dose ascending trial that took place in multiple medical centers. A total of 16 healthy premenopausal women (23 to 45 years of age) were randomized and received 20, 40, 80, and 160 mg TU2670 (GnRH antagonist) or placebo 7 days (±1 day) after the onset of menstrual bleeding. We performed a noncompartmental analysis for pharmacokinetic parameters and calculated relative minimum concentration values (Cmin, % Baseline) of serum pharmacodynamic (PD) markers (luteinizing hormone [LH], follicle-stimulating hormone [FSH], and estradiol).Results: There were no significant differences among treatments with respect to vital signs, electrocardiography, adverse events, ovulation test results, and ultrasonography. The median Tmax of TU2670 occurred 0.75 to 1.00 hours after dosing, and concentrations then declined, with a mean apparent half-life (t1/2) of 3.0 to 5.9 hours. AUClast (17.7-417.9 ng·h/mL) and Cmax (8.1-95.4 ng/mL) increased in a dose-dependent manner. The PD analysis after a single administration of TU2670 revealed dose-dependent suppression of LH, FSH, and estradiol. Maximal suppression of the pre-dose baseline (%) was 58% to 82% at 6 to 8 hours for LH, 28% to 39% at 6 to 12 hours for FSH, and 34% to 82% at 12 to 24 hours for estradiol.Conclusion: The single administration of TU2670 in healthy premenopausal women was well tolerated and resulted in the dose-dependent suppression of LH, FSH, and estradiol, suggesting rapid and significant inhibition of pituitary and ovarian hormones. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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