Galapagos Biotech Limited, Cambridge, UK.
Galapagos, Mechelen, Belgium.
Clin Pharmacol Drug Dev. 2021 Sep;10(9):994-1006. doi: 10.1002/cpdd.955. Epub 2021 May 7.
GLPG1205 is a modulator of GPR84, a G-protein-coupled receptor reported to be associated with several diseases. Safety, tolerability, pharmacokinetics, and pharmacodynamics of GLPG1205 in healthy subjects were evaluated in 2 randomized, double-blind, placebo-controlled, single-site, phase 1 studies. In study 1, 16 (aged 21-48 years) and 24 (24-50 years) healthy men received single doses of GLPG1205 10 to 800 mg, and GLPG1205 50, 100, or 200 mg once daily for 14 days, respectively, or placebo. Study 2 evaluated the effect of aging on GLPG1205 pharmacokinetics: 24 healthy men (aged 37-83 years), weight-matched into 3 age cohorts (65-74, ≥75, and 18-50 years), received GLPG1205 50 mg or placebo once daily for 14 days; an open-label part of this study evaluated a GLPG1205 250-mg loading dose followed by 50 mg once daily for 13 days in 8 healthy men (aged 68-74 years). Single (up to 800 mg) and multiple (maximum tolerated dose 100 mg once daily) GLPG1205 doses had favorable safety and tolerability profiles. After single administration of GLPG1205, median time to occurrence of maximum observed plasma concentration and arithmetic mean apparent terminal half-life ranged from 2.0 to 4.0 and from 30.1 to 140 hours, respectively. Age did not affect GLPG1205 exposure. GPR84 receptor occupancy with GLPG1205 vs placebo confirmed target engagement. These results support further clinical development of GLPG1205.
GLPG1205 是 GPR84 的调节剂,GPR84 是一种与多种疾病相关的 G 蛋白偶联受体。在两项随机、双盲、安慰剂对照、单中心、I 期研究中评估了 GLPG1205 在健康受试者中的安全性、耐受性、药代动力学和药效学。在研究 1 中,16 名(年龄 21-48 岁)和 24 名(24-50 岁)健康男性分别单次接受 GLPG1205 10 至 800mg 和 GLPG1205 50、100 或 200mg,每天一次,共 14 天,或安慰剂。研究 2 评估了年龄对 GLPG1205 药代动力学的影响:24 名健康男性(年龄 37-83 岁),按体重分为 3 个年龄组(65-74、≥75 和 18-50 岁),每天接受 GLPG1205 50mg 或安慰剂一次,共 14 天;本研究的开放标签部分评估了 8 名健康男性(年龄 68-74 岁)单次给予 GLPG1205 250mg 负荷剂量,随后每天给予 GLPG1205 50mg 共 13 天。单次(高达 800mg)和多次(最大耐受剂量为每天 100mg)GLPG1205 剂量具有良好的安全性和耐受性。GLPG1205 单次给药后,最大观察到的血浆浓度和算术平均表观终末半衰期的中位达峰时间分别为 2.0-4.0 和 30.1-140 小时。年龄不影响 GLPG1205 的暴露。与安慰剂相比,GLPG1205 对 GPR84 受体的占有率证实了其靶标结合。这些结果支持 GLPG1205 的进一步临床开发。