Overview

A Study in Healthy People to Compare 3 Different Formulations of Apremilast Tablets Taken With or Without Food

Status:
Terminated
Trial end date:
2021-08-18
Target enrollment:
Participant gender:
Summary
The aim of this trial is to establish bioequivalence between EU-, US- and Japan-sourced Otezla® tablet formulations to assure comparability of results from Phase III trials of BI 730357 (new oral agent for treatment of psoriasis as well as other T helper 17 cells (Th17)-mediated diseases) regardless of whether only the EU-sourced Otezla® or EU and US-sourced Otezla®/Japan-sourced Otezla® have been used as an active comparator.
Phase:
Phase 1
Details
Lead Sponsor:
Boehringer Ingelheim
Treatments:
Apremilast
Thalidomide