WHO ICTRP trial

A phase 1 pharmacokinetic study to assess and compare the relative…

NL-OMON50260 · Overview of Medical Research in the Netherlands (NL-OMON) · Not Recruiting

Key facts

Trial ID NL-OMON50260
Public title A phase 1 pharmacokinetic study to assess and compare the relative bioavailability of a capsule and a tablet formulation of YTX-7739 following single oral doses administered with and without food in Healthy Volunteers
Scientific title A phase 1 pharmacokinetic study to assess and compare the relative bioavailability of a capsule and a tablet formulation of YTX-7739 following single oral doses administered with and without food in Healthy Volunteers - YTX-7739 formulation study
Primary sponsor Yumanity Therapeutics
Registry Overview of Medical Research in the Netherlands (NL-OMON)
Recruitment status Not Recruiting
Study type Interventional
Countries The Netherlands
Conditions Parkinson's Disease;10028037;Parkinson's Disease
Interventions Treatment period 1: 30 mg YTX-7739 tablet formulation (2 tablets of 15mg). Treatment period 2: 30 mg YTX-7739 capsule formulation (2 capsules, 1x25mg, 1x5 mg) Treatment period 3: 30 mg YTX-7739 tablet formulation (2 tablets of 15mg), after…
Registration date Jan 6, 2022
Target size 16
Secondary IDs 2021-004754-28;NL78956.056.21
Registry page onderzoekmetmensen.nl

At a glance

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