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PK, PD, Tolerability and Safety of MDPK67b in Healthy Volunteers

2021年4月8日 更新者:Med Discovery SA

Phase I Clinical Trial of the KLK Inhibitor MDPK67b to Assess Its Pharmacokinetic, Pharmacodynamic, Tolerability and Safety Profile in Healthy Male Volunteers

This is a Phase I, single centre, prospective, randomized, alternating panels, ascending doses with interspersed placebo, double-blind, crossover trial.

The trial will include 8 volunteers divided into 2 panels (A and B) investigated in alternance, each submitted to 4 investigation periods following a crossover design in double blind, with ascending intravenous doses of MDPK67b and an interspersed placebo.

The ascending dose sequence ranges from 2 to 48 mg, with 2-fold increase steps (3 to 4- fold increase steps in each individual volunteer). Three single doses will be administered at a minimum of 2 weeks intervals during the first 3 periods, and finally during the last period 4 repeated doses will be administered at a three days intervals, using either the highest dose of the ascending sequence (i.e. 24 or 48 mg) or the maximal tolerated dose (if it has been exceeded in the ascending sequence of single doses).

研究概览

地位

完全的

研究类型

介入性

注册 (实际的)

8

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Lausanne、瑞士
        • Centre Hospitalier Universitaire Vaudois (CHUV) - Division of Clinical Pharmacology

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 45年 (成人)

接受健康志愿者

有资格学习的性别

男性

描述

Inclusion Criteria:

  1. Healthy male subjects aged between 18 and 45 years
  2. Body weight (BW) ranging between 55 and 95 kg, providing body mass index (BMI) is between 18 and 29 kg/m2
  3. Absence of significant findings in the medical history and physical examination as judged by the investigator, especially for cardiovascular, pulmonary, haematological and nervous systems
  4. Absence of significant laboratory abnormalities as judged by the investigator. Gilbert's syndrome (increased total and unconjugated bilirubin when fasting) will be accepted if mild
  5. 12-lead ECG without significant abnormalities
  6. Negative urine drug screen (amphetamines, benzodiazepines, cannabis, cocaine, opiates)
  7. Negative alcohol breath test
  8. Ability to understand the procedures, agreement to participate and willingness to give written informed consent
  9. Co-operative attitude and availability for scheduled visits over the entire study period.
  10. The subjects will have to refrain from travels outside Europe over the whole study duration.

Exclusion Criteria:

  1. History of major cardiovascular, pulmonary, hepatic, immunological, renal, haematological, gastrointestinal, genitourinary, neurological, or rheumatologic disorders
  2. Active diseases of any type, including inflammatory disorders and infections. Mild acne is permissible providing no systemic or local treatment is provided or planned (except for cleaning lotions)
  3. History of significant allergy or asthma. Allergic rhinitis or conjunctivitis is acceptable if non symptomatic when starting the study and if symptoms are not anticipated to occur during the study to a point that would require corticosteroid therapy (e.g. in case of annual use)
  4. History of cardiovascular dysfunction if considered as clinically relevant (conduction abnormality, arrhythmia, bradycardia, angina pectoris, cardiac hypertrophy unless elicited by training, pulmonary embolism)
  5. Hypertension defined as supine blood pressure >150/90 mmHg or recurrent hypotensive events considered as clinically relevant or documented orthostatic hypotension
  6. Any clinically significant coagulation disorder, based on either clinical manifestations (abnormal bleeding etc.) or abnormal laboratory values (platelet count, TP, aPTT, Thrombin time and fibrinogen).
  7. Sick sinus syndrome, known long QT syndrome, reproducible observation of QTc >440 ms or of pronounced sinus bradycardia (<40 bpm)
  8. Intense sport activities. Moderate sport is acceptable and activities should remain fairly constant throughout the study
  9. Any clinically significant laboratory value on screening that are not within normal range on single repeat (Gilbert's syndrome acceptable if mild)
  10. Positive hepatitis B or C antigen screen
  11. Positive HIV antibody screen or screen not performed
  12. Any recent acute illness or sequelae thereof which could expose the subject to a higher risk or might confound the results of the study
  13. Treatment in the previous three months with any drug known to have well-defined potential for toxicity to a major organ
  14. History of hypersensitivity to any drug if considered as serious
  15. Use of any medication the week prior to study or as based on 5 serum half-life rule and throughout study, including aspirin or other over-the-counter (OTC) preparation. Paracetamol is permissible before and during study as a rescue medication but only with investigator's permission.
  16. Participation in a clinical investigation or blood donation of 500 ml within the past 3 months
  17. History of relevant alcohol or drug abuse
  18. Smoking. Consumption of ≤5 cigarettes/day or equivalent is acceptable providing the subject can refrain from smoking from one week before and during the whole study duration
  19. Consumption of a large quantity of coffee, tea, chocolate (more than 4 cups/day) or equivalent (Cola drinks)
  20. Present consumption of a large quantity of alcohol or wine (>0.5 L wine/day) or equivalent, (equivalent to more than 35 g ethanol per day).
  21. Psychological status which could impact on subject's ability to give informed consent
  22. Any feature of subject's medical history or present condition which, in the investigator's opinion, could confound the results of the study, complicate its interpretation, or represent a potential risk for the subject.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂
Two subgroups (Panel A and Panel B) of four subjects were to be randomly allocated either to placebo or to three increasing doses of MDPK67b, administered as single infusion at intervals of at least two weeks during the first three periods with the last period involving four repeated doses administered at three-day intervals.
有源比较器:MDPK67b
Two subgroups (Panels A and Panel B) of four subjects were to be randomly allocated either to placebo or to three increasing doses of MDPK67b, administered as single infusion at intervals of at least two weeks during the first three periods with the last period involving four repeated doses administered at three-day intervals.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Incidence of Adverse Events (AEs)
大体时间:Week 8
Subjects were assessed for AEs at each visit.
Week 8
MDPK67b serum level
大体时间:Up to 144 hours after drug administration
Serum concentrations of MDPK67b were measured using an ELISA method.
Up to 144 hours after drug administration

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2017年2月21日

初级完成 (实际的)

2017年6月7日

研究完成 (实际的)

2017年6月7日

研究注册日期

首次提交

2021年3月29日

首先提交符合 QC 标准的

2021年4月8日

首次发布 (实际的)

2021年4月9日

研究记录更新

最后更新发布 (实际的)

2021年4月9日

上次提交的符合 QC 标准的更新

2021年4月8日

最后验证

2021年4月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

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MDPK67b的临床试验

3
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