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临床试验/NCT03067363
NCT03067363终止1 期

Assessment of Safety, Tolerability and Pharmacokinetics of Single Ascending Subcutaneous Doses of MOR107 in Healthy Male Subjects and Pharmacodynamics in Healthy Male Subjects on a Low Sodium Diet

Alan Richardson1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2017年2月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
终止
发起方
入组人数
24
试验地点
1
主要终点
Incidence of treatment-emergent adverse events (safety and tolerability)

研究概览

简要总结

This is the first in human study of MOR107. It is a 2 part, single centre, double-blind, randomised, placebo-controlled study in healthy male subjects. Part 1 is a single ascending dose study, and Part 2 is a parallel group, dose range finding study in healthy male subjects on a low sodium diet.

详细描述

MOR107 is an angiotensin 2 receptor (AT2R) agonist with the potential to treat a wide range of diseases through activation of the protective arm of the renin-angiotensin system.

In this study MOR107 will be administered to humans for the first time.

The study will enroll healthy male subjects and is split into two sequential parts, both of which have a single centre, double-blind, randomised, placebo-controlled design.

Part 1 will evaluate the safety, tolerability and pharmacokinetics (PK) of single ascending doses of MOR107.

Part 2 will evaluate the pharmacodynamics, safety, tolerability and PK of three different doses of MOR107 in healthy male subjects who will be fed a low sodium diet in order to increase AT2R expression.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Healthy males
  • Age 18 to 45 years of age
  • Body mass index of 18.0 to 32.0 kg/m2
  • For Part 2, subjects must have at least a 25% reduction in 24 hour urinary sodium excretion on Day -2 compared with admission

排除标准

  • Subjects who have received any IMP in a clinical research study within the previous three months
  • Regular alcohol consumption >21 units per week (1 unit = ½ pint beer, 25 mL of 40% spirit or a 125 mL glass of wine)
  • Current smokers and those who have smoked within the last 12 months. A breath carbon monoxide reading of greater than 10 ppm at screening/admission
  • Current smokers of e-cigarettes and nicotine replacement products and those who have smoked these products within the last 12 months
  • Clinically significant abnormal biochemistry, haematology or urinalysis as judged by the investigator
  • Positive drugs of abuse test result
  • Positive hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab) or human immunodeficiency virus (HIV) results
  • History of psychiatric disorder, cardiovascular, renal, hepatic, chronic respiratory or gastrointestinal disease as judged by the investigator
  • Serious adverse reaction or serious hypersensitivity to any drug or the formulation excipients

研究组 & 干预措施

Part 2: MOR107 high dose

Experimental

MOR107 high dose single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: Low sodium diet (Other)

Part 1, MOR107 Dose level 1

Experimental

MOR107, single subcutaneous injection

干预措施: MOR107 (Drug)

Part 1, MOR107 Dose level 2

Experimental

MOR107, single subcutaneous injection

干预措施: MOR107 (Drug)

Part 1, MOR107 Dose level 3

Experimental

MOR107, single subcutaneous injection

干预措施: MOR107 (Drug)

Part 1, MOR107 Dose level 4

Experimental

MOR107, single subcutaneous injection

干预措施: MOR107 (Drug)

Part 1, MOR107 Dose level 5

Experimental

MOR107, single subcutaneous injection

干预措施: MOR107 (Drug)

Part 1, MOR107 Dose level 6

Experimental

MOR107, single subcutaneous injection

干预措施: MOR107 (Drug)

Part 1, Placebo

Placebo Comparator

Placebo, single subcutaneous injection

干预措施: Placebo (Drug)

Part 2: MOR107 low dose

Experimental

MOR107 low dose single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: MOR107 (Drug)

Part 2: MOR107 low dose

Experimental

MOR107 low dose single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: Low sodium diet (Other)

Part 2: MOR107 medium dose

Experimental

MOR107 medium dose single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: MOR107 (Drug)

Part 2: MOR107 medium dose

Experimental

MOR107 medium dose single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: Low sodium diet (Other)

Part 2: MOR107 high dose

Experimental

MOR107 high dose single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: MOR107 (Drug)

Part 2: Placebo

Placebo Comparator

Placebo single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: Placebo (Drug)

Part 2: Placebo

Placebo Comparator

Placebo single subcutaneous injection and low sodium diet for 6 days before dosing and 2 days after dosing

干预措施: Low sodium diet (Other)

结局指标

主要结局

Incidence of treatment-emergent adverse events (safety and tolerability)

时间窗: Up to 10 days post-dose

Reporting of adverse events, physical examination, injection site assessment, vital signs, ECG, and clinical chemistry, haematology and urinalysis

次要结局

  • Concentration of MOR107 at 12 hours post-dose (C12)(12 hours post-dose)
  • Area under the curve from 0 time to last measurable MOR107 concentration (AUC0-t)(Up to 48 hours post-dose)
  • MOR107 Cmax normalised for dose (Cmax/D)(Up to 48 hours post-dose)
  • Cumulative amount of MOR107 excreted in the urine, expressed as a percentage of the administered dose (CumAe%)(Up to 48 hours post-dose)
  • Time from dosing at which the maximum MOR107 concentration was observed (Tmax)(Up to 48 hours post-dose)
  • Concentration of MOR107 at 24 hours post-dose (C24)(24 hours post-dose)
  • MOR107 AUC(0-t) normalised for dose (AUC[0-t]/D)(Up to 48 hours post-dose)
  • Amount of MOR107 excreted in the urine over a specified period of time after dosing (Ae)(Up to 48 hours post-dose)
  • Amount of MOR107 excreted in the urine over a specified period of time after dosing, expressed as a percentage of the administered dose (Ae%)(Up to 48 hours post-dose)
  • Renal clearance: the apparent volume of plasma cleared per unit time via renal elimination (CLr)(Up to 48 hours post-dose)
  • Area under the curve from 0 time to infinity for MOR107 (AUC0-inf)(Up to 48 hours post-dose)
  • Percentage of AUC(0-inf) for MOR107 extrapolated beyond last measured time point (AUC%extrap)(Up to 48 hours post-dose)
  • Slope of the apparent elimination phase for MOR107 (Lambda-z)(Up to 48 hours post-dose)
  • Cumulative amount of MOR107 excreted in the urine (CumAe)(Up to 48 hours post-dose)
  • Maximum observed MOR107 concentration (Cmax)(Up to 48 hours post-dose)
  • MOR107 AUC(0-inf) normalised for dose (AUC[0-inf]/D)(Up to 48 hours post-dose)
  • Apparent elimination half-life for MOR107 (T-half)(Up 48 hours post-dose)

研究者

发起方
Alan Richardson
申办方类型
Industry
责任方
Sponsor Investigator
主要研究者

Alan Richardson

Clinical Project Manager

LanthioPep BV

研究点 (1)

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