39
Participants
Start Date
May 29, 2018
Primary Completion Date
August 17, 2019
Study Completion Date
August 21, 2019
Lu AF28996 solution
"Oral solution (0.1-0.2 mg/mL)~Following each cohort, a dosing conference will be held where tolerability, safety and preliminary PK results from the previous cohorts will be reviewed before deciding on the next doses"
Lu AF28996 capsule
hard capsule orally QD: one dose lower than the highest dose level in part A
QPS Netherlands BV, Groningen
H. Lundbeck A/S
INDUSTRY