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临床试验/NL-OMON44567
NL-OMON44567已完成不适用

A randomized, double blind, placebo-controlled single ascending dose study on the safety, tolerability, pharmacokinetics and pharmacodynamics of ACT017 in healthy volunteers - ACT-CS-001 (CS0278)

Acticor Biotech SAS0 个研究点目标入组 48 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
48

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Males or non-pregnant, non-breastfeeding females, aged *18 and 65 years. Female subjects must be of non-childbearing potential, defined as pre-menopausal females with a documented tubal ligation, hysterectomy or bilateral oophorectomy; or as post-menopausal females defined as 12 months amenorrhea and follicle stimulating hormone (FSH) levels >40 IU/L.
  • 2. Body mass index (BMI) *18 kg/m2 and 30 kg/m2 at screening.
  • 3. A resting pulse *40 beats per minute (bpm) and *100 bpm at screening and on Day -1.
  • 4. A resting systolic blood pressure of *150 mmHg and a resting diastolic blood pressure of *95 mmHg at screening and on Day -1.
  • 5. Baseline laboratory test values within reference ranges based on the blood and urine samples taken at screening and on Day -1. Out of normal ranges values may be accepted by the Investigator, if not clinically significant. Values for hemostasis and coagulation blood test, for bleeding time and platelet aggregation should be normal.

排除标准

  • 1. The subject has a history of hemorrhagic disease or venous or arterial thrombotic disease.
  • 2. The subject has a history or presence of any disorder with an increased risk of bleeding (e.g. ulcus pepticus, hemorrhoids).
  • 3. The subject has used drugs modifying hemostasis or platelet function within the last month prior to administration of the study drug (i.e. aspirin, antiplatelet drugs, anti-vitamin K drugs and anticoagulant drugs).
  • 4. The subject has used anti-histamines within the last month prior to administration of the study drug.
  • 5. The subject has taken prescription or non-prescription medication, herbal remedies, vitamins or minerals within 2 weeks prior to administration of the study drug (or within 5 half-lives prior to administration of the study drug for any medication ingested, whichever is longer).

研究者

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