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Safety, tolerability, and pharmacokinetics of HRS9432(A) injection in healthy Chinese subjects: a phase-I randomized, double-blind, dose escalation, placebo-controlled study.
Yan, Xin; Huang, Yuanyuan; Xie, Jinlian; Wu, Qian; Yang, Shuang; Yang, Xiaoyan; Chen, Honghui; Huang, Jie; Yang, Guoping.
Afiliación
  • Yan X; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan, China.
  • Huang Y; Jiangsu Hengrui Pharmaceuticals Co, Ltd, Shanghai, China.
  • Xie J; Clinical Pharmacology Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
  • Wu Q; Clinical Pharmacology Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
  • Yang S; Clinical Pharmacology Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
  • Yang X; Clinical Pharmacology Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
  • Chen H; Clinical Pharmacology Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
  • Huang J; Clinical Pharmacology Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
  • Yang G; Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan, China.
Antimicrob Agents Chemother ; 68(7): e0052424, 2024 Jul 09.
Article en En | MEDLINE | ID: mdl-38899917
ABSTRACT
HRS9432(A) is a long-acting echinocandin antifungal medication primarily used to treat invasive fungal infections, particularly invasive candidiasis. The safety, tolerability, and pharmacokinetic characteristics of HRS9432(A) injection were investigated in a randomized, double-blind, placebo-controlled, single- and multiple-ascending-dose Phase I study involving 56 healthy adult subjects. Doses ranging from 200 to 1200 mg were administered. Safety was continually monitored, including adverse events, clinical laboratory examinations, vital signs, 12-lead electrocardiograms, and physical examinations, while the pharmacokinetic profile within the body was evaluated. The results indicated that concentrations of HRS9432 peaked immediately after infusion, demonstrating essentially linear pharmacokinetic characteristics within the dosage range of 200-1,200 mg. It exhibited a low clearance rate and an extended half-life, with a clearance of approximately 0.2 L/h, a volume of distribution of around 40 L, and a half-life of approximately 140h following a single dose. The accumulation index for AUC0-τ after multiple doses ranged from 1.41 to 1.75. No severe adverse events occurred during the study, and the severity of all adverse events was mild or moderate. Therefore, the intravenous administration of HRS9432(A) in healthy Chinese adult subjects, either as multiple infusions of 200 to 600 mg (once a week, four doses) or as a single infusion of 900-1,200 mg, demonstrated overall good safety and tolerability. The pharmacokinetic exhibited essentially linear characteristics in the body, supporting a weekly dosing frequency for clinical applications and providing additional options for the treatment or prevention of invasive fungal infections. CLINICAL TRIALS This study is registered with the International Clinical Trials Registry Platform as ChiCTR2300073525.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Voluntarios Sanos / Antifúngicos Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Antimicrob Agents Chemother Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Voluntarios Sanos / Antifúngicos Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Antimicrob Agents Chemother Año: 2024 Tipo del documento: Article País de afiliación: China