A Relative Bioavailability Study of FOR-6219 in Capsule and Tablet Formulations

Relative Bioavailability Clinical Trial

Official title:
A Phase 1, Randomised, Open-Label, Three-way, Three-period, Crossover Relative Bioavailability Study to Assess the Single-Dose Pharmacokinetics of FOR-6219 in Capsule and Tablet Formulations in Postmenopausal Women

Status Completed

Clinical Trial Summary

This is a phase 1, randomised, open-label, three-way, three-period, crossover relative bioavailability study to assess the single-dose pharmacokinetics of FOR-6219 in capsule and tablet formulations in postmenopausal women. The effect of high-fat food on the pharmacokinetics of the tablet formulation will also be evaluated. A total of twelve, post-menopausal women, will be randomised to receive a single oral dose of FOR-6219 in three treatment periods: capsule formulation (fasted); tablet formulation (fed); tablet formulation (fasted)

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Relative Bioavailability

Clinical Trial Details

NCT number	NCT04686669
Study type	Interventional
Source	Forendo Pharma Ltd
Contact
Status	Completed
Phase	Phase 1
Start date	December 10, 2020
Completion date	January 16, 2021

View Details

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