Stopped: Portfolio proritisation
This is the first clinical trial with LEO 142397. The purpose of the trial is to assess the safety and tolerability of LEO 142397, along with the pharmacokinetics (what the body does to the drug) and the pharmacodynamics (what the drug does to the body) in healthy people. The trial consists of 2 parts: * In Part 1, participants will receive a single dose of LEO 142397. There will be up to 8 different dose groups. * In Part 2, participants will receive a daily dose of LEO 142397 for 14 days. There will be up to 6 different dose groups. Each participant will be enrolled into 1 dose group in either Part 1 or Part 2.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Part 1. Number of treatment-emergent adverse events per subject
Timeframe: From Day 1 (postdose) up to Day 8
Part 1. Having clinically significant abnormalities in systolic blood pressure
Timeframe: From Day 1 (postdose) up to Day 8
Part 1. Having clinically significant abnormalities in diastolic blood pressure
Timeframe: From Day 1 (postdose) up to Day 8
Part 1. Having clinically significant abnormalities in heart rate
Timeframe: From Day 1 (postdose) up to Day 8
Part 1. Having clinically significant abnormalities in oral body temperature
Timeframe: From Day 1 (postdose) up to Day 8
Part 1. Having an abnormal ECG
Timeframe: From Day 1 (postdose) up to Day 8
Part 2. Number of treatment-emergent adverse events per subject
Timeframe: From Day 1 (postdose) up to Day 21
Part 2. Having clinically significant abnormalities in systolic blood pressure
Timeframe: From Day 1 (postdose) up to Day 21
Part 2. Having clinically significant abnormalities in diastolic blood pressure
Timeframe: From Day 1 (postdose) up to Day 21
Part 2. Having clinically significant abnormalities in heart rate
Timeframe: From Day 1 (postdose) up to Day 21
Part 2. Having clinically significant abnormalities in oral body temperature
Timeframe: From Day 1 (postdose) up to Day 21
Part 2. Having an abnormal ECG
Timeframe: From Day 1 (postdose) up to Day 21