An open-label, active-controlled study of NPC-25 in patients with hypozincemia (noninferiority study) (NPC-25-3)

Nobelpharma Co., Ltd.0 个研究点目标入组 190 人开始时间: 2022年1月20日最近更新: 2025年4月14日

试验速览

暂无简介。

•Patients who have provided written informed consent and are confirmed to meet the following criteria (1) and (2) at the time of enrollment.
•(1) Patients whose serum zinc concentrations (measured at institutions) both at the time of enrollment and within 8 weeks before the start of treatment are less than 70 micro g/dL
•(2) Patients weighing at least 30 kg who are capable of taking tablets orally at the time of providing informed consent, regardless of sex and inpatient or outpatient status

•Patients falling under any of the following criteria at the time of enrollment will be excluded.
•(1) Patients with fulminant hepatitis
•(2) Patients with malignant tumors
•(3) Patients with serious heart, blood, kidney or pancreatic disease, or the like
•(4) Patients with serum albumin levels of less than 2.8 g/dL
•(5) Patients with serum copper concentrations below the lower limit of the reference range
•(6) Patients who have allergies or hypersensitivity to zinc-containing preparations (including supplements)
•(7) Patients who have taken zinc-containing preparations or zinc-containing supplements that are prohibited from being used concomitantly within 12 weeks before enrollment.
•(8) Patients who are or may possibly be pregnant, or wish to become pregnant during the study period
•(9) Patients who participated in other clinical trials within 12 weeks before enrollment.
•(10) Patients whose participation in the study is considered inappropriate by the investigator (subinvestigator).

Proportion of subjects maintaining target serum zinc concentration

时间窗: within 24 weeks of the start of the treatment

The proportion of subjects who become able to maintain the target serum zinc concentration range (80 to <200 micro g/dL) for 8 weeks at the same dose

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