drugset / Trial / NCT03961932

Safety and Pharmacokinetics of Linzagolix in Female Subjects With Normal and Impaired Renal Function

NCT03961932

Phase 1 Completed 33 enrolled ObsEva SA
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The primary objective of this study is to assess the pharmacokinetics (PK) of linzagolix in subjects with varying degrees of impaired renal function compared to matched control subjects with normal renal function

Timeline

Start
2019-05-15
Primary completion
2020-01-22
Completion
2020-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject linzagolix Unknown 200 mg Oral