A Phase I Bridging Study to Evaluate the PK, PD, Safety and Tolerability of SR1375 in Healthy Subjects

Shanghai SIMR Biotechnology Co., Ltd.1 个研究点分布在 1 个国家目标入组 32 人开始时间: 2022年6月24日最近更新: 2024年11月28日

适应症

干预措施

试验速览

阶段: 1 期
状态: 已完成
发起方: Shanghai SIMR Biotechnology Co., Ltd.
入组人数: 32
试验地点: 1
主要终点: Cmax

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This is a randomized, double-blind, placebo-controlled phase I bridging study to evaluate the PK, PD, safety and tolerability of SR1375 in healthy subjects.

详细描述

The study is a Phase I study to evaluate the PK, PD, safety, and tolerability of SR1375 in healthy volunteers. The study will include 3 single-ascending-dose (SAD) cohorts and 1 multiple-dose cohorts (Part A and part B respectively), a total of 4 cohorts, and each cohort includes 3 stages: screening and baseline, treatment and safety monitoring, and safety follow-up.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Sequential
主要目的: Treatment
盲法: Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围: 18 Years 至 45 Years（Adult）
性别: All
接受健康志愿者: 是

入选标准

•Healthy males and females who are 18 to 45 years of age.
•Based on medical history, physical examination, laboratory examination, chest CT scan, abdominal B-ultrasound, vital signs and ECG, the investigator considered that the results were normal or abnormal but no clinical significance.
•Bodyweight of male > 50 kg, Bodyweight of female > 45 kg and body mass index (BMI) between 18 and 28 kg/m
•Male subjects must agree to use a highly effective contraceptive method from signing the consent form until at least 90 days after the last dose of study drug, and must be willing not to donate sperm.
•Healthy female volunteers must be:
•i. Of non-childbearing potential(with a documented tubal ligation, bilateral salpingectomy, hysterectomy, or menopause for more than 1 year) ii. Of childbearing potential, must have a negative pregnancy test at the screening visit (blood test), must agree to use a highly effective contraceptive method from signing the consent form until at least 30 days after the last dose of study drug.
•Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

排除标准

•History of hypercoagulable state or history of thrombosis.
•Current or chronic history of liver disease or known hepatic or biliary abnormalities.
•History of sensitivity to any of the investigational medicinal products (IMPs), or components thereof or a history of drug or other allergy that, in the opinion of the Investigator or Medical Monitor, contraindicates participation.
•History of asthma (excluding resolved childhood asthma), severe allergic responses.
•History of significant drug abuse within one year of screening.
•Except for topical (no significant systemic exposure) permitted, use of the following combination agents will be excluded:
•Use of prescription drugs within 14 days prior to initial administration, or within 7 days or five half-lives of the medication (whichever is longer) prior to the first study drug administration, except occasional use of paracetamol (up to a maximum of 2000 mg per day of paracetamol and per local or national abelling).
•Use the health supplement 7 days or 5 half-life before the first administration of the investigational drug.
•Use of depot injection or subcutaneous implantation drugs within 3 months prior to the first study drug administration.
•Received vaccine within 1 month prior to the first administration of the investigational drug.
•A positive Hepatitis B surface antigen, positive Hepatitis C antibody and positive test for human immunodeficiency virus (HIV) antibody or treponema pallidum antibody.
•A positive drug/alcohol result.
•History of regular alcohol consumption within 6 months of screening defined as:
•an average weekly intake of >14 units (1 unit of alcohol ≈360 mL beer or 45 mL 40% alcohol spirits or 150 mL wine), or abstain from alcohol during the study.
•Within 6 months of screening, smoking more than 5 cigarettes(including e- cigarettes).
•Donation or lost in excess of 400 mL of blood within 2 months of Day 1 or donation of plasma within 14 days of Day
•The subject has participated in a clinical trial within 3 months of receiving IMP.
•Unable to refrain from consumption of Seville oranges, grapefruit or grapefruit juice within 24h prior to the first dose of IMP until the Safety Follow-up visit.
•Breast-feeding and/or lactating subject.
•Any reason which, in the opinion of the Investigator, would prevent the subject from participating in the study.

研究组 & 干预措施

SR1375 capsules

Experimental

Ascending single and multiple doses of SR1375 orally

干预措施: SR1375 capsules (Drug)

Placebo

Placebo Comparator

Ascending single and multiple doses of SR1375 placebo orally

干预措施: Placebo (Other)