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Clinical Trial Summary

The study's primary objective is to determine the bioavailability of two solid formulations of IP2015 compared to a liquid formulation of IP2015 in healthy male subjects


Clinical Trial Description

It is planned to include 12 subjects. Each subject will take part in three treatment periods, in which they will receive a single dose of IP2015 liquid and then to different IP2015 solid formulations, respectively, in each treatment period. Overall, each subject will receive each treatment once only. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05728671
Study type Interventional
Source Initiator Pharma
Contact Mikael Thomsen, PhD
Phone 23276134
Email mt@initiatorpharma.com
Status Not yet recruiting
Phase Phase 1
Start date February 16, 2023
Completion date July 20, 2023

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