drugset / Trial / NCT06954493

Pharmacokinetic Study in Healthy Lactating Women Exposed to Ibrexafungerp

NCT06954493

Phase 1 Completed 5 enrolled Scynexis, Inc.
NaSingle-groupOpen-labelOther

Summary

This is a pharmacokinetic evaluation of lactating women after receiving two doses of Ibrexafungerp. The study population included healthy lactating females who were at least 10 days postpartum with a fully established milk supply and were between the ages of 18 and 50 years at the time of screening

Timeline

Start
2023-07-12
Primary completion
2023-11-01
Completion
2023-11-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ibrexafungerp Small molecule 300 mg Oral