Overview

Comparing the Extent to Which AQ280 is Made Available in the Body After Single Oral Doses of a Capsule Formulation Versus a Tablet for Oral Suspension Formulation

Status:
COMPLETED
Trial end date:
2025-07-22
Target enrollment:
Participant gender:
Summary
This is a Phase 1, investigator- and participant-blinded, placebo-controlled, randomized, crossover study to compare bioavailability of AQ280 following single oral doses of a capsule formulation versus a tablet for oral suspension formulation in healthy participants.
Phase:
PHASE1
Details
Lead Sponsor:
AQILION AB
Treatments:
Suspensions