Last updated on September 2016

Study of Ulipristal Acetate in Female Patients With Moderately or Severely Impaired Renal Function Compared With Matched Healthy Female Subjects

Brief description of study

This study is designed to observe the effect of renal function on the pharmacokinetic, safety, and tolerability profiles of Ulipristal acetate following administration of a single oral dose of a 10 mg Ulipristal acetate tablet.

Clinical Study Identifier: NCT02634437

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