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Clinical trial

A First-In-Human Phase I Study in 3 Parts: Randomized, Double-blind, Placebocontrolled, Sequential Group Investigation of the Safety, Tolerability, Pharmacokinetics of AEF0217 After Oral, Single and Multiple Ascending Doses, and an Open Label, Cross-over Investigation of the Effect of Food on the Bioavailability of AEF0217 in Healthy Volunteers.

NCT05170737 is registered in ClinicalTrials.gov with Aelis Farma as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A First-In-Human Phase I Study in 3 Parts: Randomized, Double-blind, Placebocontrolled, Sequential Group Investigation of the Safety, Tolerability, Pharmacokinetics of AEF0217 After Oral, Single and Multiple Ascending Doses, and an Open Label, Cross-over Investigation of the Effect of Food on the Bioavailability of AEF0217 in Healthy Volunteers.
Lead sponsor
Aelis Farma
Phase
Phase 1
Overall status
Completed
Start date
October 1, 2021
Completion date
June 28, 2022
Enrollment
68 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

safety, tolerability, pharmacokinetics of aef0217