跳至主要内容
临床试验/NL-OMON50697
NL-OMON50697已完成不适用

A single-center, open-label, fixed-sequence Phase 1 trial to evaluate the effect of multiple doses of pritelivir on the pharmacokinetics of substrates for CYP2C9, CYP2B6, CYP3A4 and OATP2B1 - Pritelivir DDI study with celiprolol, flurbiprofen, bupropion and midazolam

AiCuris Anti-infective Cures AG0 个研究点目标入组 16 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
16

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 64(—)

入选标准

  • - Subject has been informed both verbally and in writing about the objectives
  • of the clinical trial, the methods, and the potential risks and the discomfort
  • to which he/she may be exposed and has given written consent to participation
  • in the trial prior to trial start and any trial related procedure.
  • - Healthy male and female subjects of any ethnic origin, aged between 18 and 55
  • years (inclusive). Assessed as healthy based on a pre-trial examination
  • including medical history,
  • physical examination, blood pressure, pulse rate, body temperature, ECG
  • assessment, and clinical laboratory results.
  • - In women negative serum β-HCG (beta-human chorionic gonadotropin) test at
  • screening and
  • negative urine β-HCG test on Day -1.
  • - Subject agrees to pharmacogenetic blood sampling.
  • - Normal body weight as evidenced by a Body Mass Index (BMI) >=18.0 and <=30.0
  • kg/m2, and a body weight >=50.0 kg at Screening.
  • More criteria apply

排除标准

  • 1. History or current evidence of clinically relevant allergies or idiosyncrasy
  • to drugs or food.
  • 2. History of allergic reactions to any active or inactive ingredient(s) of the
  • Investigational Medicinal Products (IMPs).
  • 3. History or current evidence of any clinically relevant cardiovascular,
  • pulmonary, hepatic, renal, gastrointestinal, hematological, endocrinological,
  • metabolic, neurological, psychiatric, or other disease suspected to influence
  • pharmacokinetics or safety of the IMPs.
  • 4. History of malignancy within 5 years, unless one of the following, treated
  • and considered cured: basal cell carcinoma, in situ cervical cancer, or breast
  • ductal carcinoma in situ.
  • 5. Resting pulse rate after 5 minutes in supine position at Screening and Day
  • -1: <45 or >100 beats per minute (bpm), if out of range, up to one repeat
  • assessment is allowed.
  • More criteria apply

研究者

相似试验