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Relative Bioavailability of Linaprazan for the Test Formulation vs. Reference Formulation — BA  

Pharmacokinetics Clinical Trial

Official title:
A Randomized, Single Dose, Crossover Study in Healthy Volunteers to Investigate the Relative Bioavailability of Linaprazan for a New Oral Tablet Formulation of Linaprazan Glurate, and to Assess the Effect of Food on the Pharmacokinetics of Linaprazan

Clinical Trial Summary

This is a single-center, open-label, randomized, single dose, 3-way crossover study in healthy volunteers designed to evaluate the relative bioavailability of a new oral tablet formulation of linaprazan glurate in comparison to a previously studied oral tablet formulation under fasting conditions, and to assess the effect of a high fat, high calorie meal on the pharmacokinetics (PK) of linaprazan glurate and the active substance linaprazan after the administration of the new oral tablet formulation.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05627518
Study type Interventional
Source Cinclus Pharma AG
Contact
Status Completed
Phase Phase 1
Start date November 15, 2022
Completion date January 2, 2023
View Details
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