Healthy Clinical Trial
Official title:
Interventional, Randomized, Double-blind, Sequential-group, Placebo-controlled, Single-ascending Oral Dose Study Investigating the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Properties of Lu AF95245 and Open-label Crossover Study to Investigate Intra-subject Variability, Effect of Food on Lu AF95245, and Metabolic Profile of [14C]-Lu AF95245 in Healthy Young Men
The purpose of this study is to investigate the safety and tolerability of Lu AF95245 and what the body does to Lu AF95245 after swallowing single doses of the drug
The study is divided in two parts, Part A and Part B:
Part A: interventional, randomized, double-blind, sequential-group, placebo-controlled,
single-ascending oral dose study in healthy young men.
Part A will consist of up to 6 cohorts (Cohorts A1 to A6) with 9 subjects in each cohort. In
each cohort, the subjects will be randomised to receive a single oral dose of Lu AF95245 or
placebo (ratio 6:3)
Part B: interventional, randomized, open-label, three-period crossover study to investigate
intra-subject variability, effect of food and mass balance and metabolic profile in healthy
young men. Part B will be initiated when a anticipated therapeutically relevant dose
confirmed to be safe and well-tolerated has been identified in Part A; this dose will be used
in Part B. Part B is divided into 3 dosing periods and subjects will be randomised to 1 of 3
groups (Groups B1, B2, and B3) with 4 subjects in each group and the groups will be running
in parallel.
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