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新型校正剂 GLPG2222 可增强 CFTR 的活性,在两项随机试验中,无论是否联合 ivacaftor 使用,均观察到了这一作用。

CFTR activity is enhanced by the novel corrector GLPG2222, given with and without ivacaftor in two randomized trials.

机构信息

Department of Thoracic Medicine, The Prince Charles Hospital and QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Manchester Adult Cystic Fibrosis Centre, Manchester University NHS Foundation Trust, Manchester, UK.

出版信息

J Cyst Fibros. 2019 Sep;18(5):700-707. doi: 10.1016/j.jcf.2019.04.014. Epub 2019 May 3.

Abstract

BACKGROUND

Several treatment approaches in cystic fibrosis (CF) aim to correct CF transmembrane conductance regulator (CFTR) function; the efficacy of each approach is dependent on the mutation(s) present. A need remains for more effective treatments to correct functional deficits caused by the F508del mutation.

METHODS

Two placebo-controlled, phase 2a studies evaluated GLPG2222, given orally once daily for 29 days, in subjects homozygous for F508del (FLAMINGO) or heterozygous for F508del and a gating mutation, receiving ivacaftor (ALBATROSS). The primary objective of both studies was to assess safety and tolerability. Secondary objectives included assessment of pharmacokinetics, and of the effect of GLPG2222 on sweat chloride concentrations, pulmonary function and respiratory symptoms.

RESULTS

Fifty-nine and 37 subjects were enrolled into FLAMINGO and ALBATROSS, respectively. Treatment-related treatment-emergent adverse events (TEAEs) were reported by 29.2% (14/48) of subjects in FLAMINGO and 40.0% (12/30) in ALBATROSS; most were mild to moderate in severity and comprised primarily respiratory, gastrointestinal, and infection events. There were no deaths or discontinuations due to TEAEs. Dose-dependent decreases in sweat chloride concentrations were seen in GLPG2222-treated subjects (maximum decrease in FLAMINGO: -17.6 mmol/L [GLPG2222 200 mg], p < 0.0001; ALBATROSS: -7.4 mmol/L [GLPG2222 300 mg], p < 0.05). No significant effects on pulmonary function or respiratory symptoms were reported. Plasma GLPG2222 concentrations in CF subjects were consistent with previous studies in healthy volunteers and CF subjects.

CONCLUSIONS

GLPG2222 was well tolerated. Sweat chloride reductions support on-target enhancement of CFTR activity in subjects with F508del mutation(s). Significant improvements in clinical endpoints were not demonstrated. Observed safety results support further evaluation of GLPG2222, including in combination with other CFTR modulators.

FUNDING

Galapagos NV. Clinical trial registration numbers FLAMINGO, NCT03119649; ALBATROSS, NCT03045523.

摘要

背景

囊性纤维化 (CF) 的几种治疗方法旨在纠正 CF 跨膜电导调节剂 (CFTR) 的功能;每种方法的疗效都取决于存在的突变。仍然需要更有效的治疗方法来纠正 F508del 突变引起的功能缺陷。

方法

两项安慰剂对照、2a 期研究评估了 GLPG2222,每日口服一次,共 29 天,用于纯合 F508del(FLAMINGO)或杂合 F508del 和门控突变的受试者,接受 ivacaftor(ALBATROSS)治疗。这两项研究的主要目的均为评估安全性和耐受性。次要目标包括评估药代动力学,以及 GLPG2222 对汗液氯化物浓度、肺功能和呼吸道症状的影响。

结果

FLAMINGO 和 ALBATROSS 分别纳入了 48 例和 30 例受试者。FLAMINGO 中 29.2%(14/48)的受试者和 ALBATROSS 中 40.0%(12/30)的受试者报告了与治疗相关的治疗后出现的不良事件(TEAE);大多数为轻度至中度,主要为呼吸道、胃肠道和感染事件。无因 TEAE 而死亡或停药。GLPG2222 治疗的受试者可见汗液氯化物浓度呈剂量依赖性下降(FLAMINGO 中最大下降:-17.6mmol/L[GLPG2222 200mg],p<0.0001;ALBATROSS:-7.4mmol/L[GLPG2222 300mg],p<0.05)。未报告对肺功能或呼吸道症状有显著影响。CF 受试者的血浆 GLPG2222 浓度与之前在健康志愿者和 CF 受试者中的研究一致。

结论

GLPG2222 耐受性良好。汗液氯化物减少支持 F508del 突变受试者的 CFTR 活性靶向增强。未证明临床终点有显著改善。观察到的安全性结果支持进一步评估 GLPG2222,包括与其他 CFTR 调节剂联合评估。

资金

Galapagos NV。临床试验注册号 FLAMINGO,NCT03119649;ALBATROSS,NCT03045523。

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