Overview

A Phase I Study to Assess the Pharmacokinetics of Olorofim in Subjects With Hepatic Impairment

Status:
Recruiting
Trial end date:
2021-09-30
Target enrollment:
Participant gender:
Summary
A single oral dose study to investigate the PK and safety of olorofim in mild and moderately hepatically impaired subjects compared to subjects with normal hepatic function.
Phase:
Phase 1
Details
Lead Sponsor:
F2G Biotech GmbH
F2G Ltd.
Treatments:
Olorofim