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A Study to Investigate the Repeat-dose Pharmacokinetics of a Combined Oral Contraceptive When Given Alone and in Combination With Ganfeborole in Female Participants of Non-childbearing Potential

StatusNot Yet Recruiting
PhasePhase 1
Started2026-09-01
View on ClinicalTrials.gov ↗
This study is designed to assess the pharmacokinetics (PK), safety, and tolerability of Ganfeborole and Microgynon, an oral contraceptive containing ethinylestradiol (EE) and levonorgestrel (LNG), when Microgynon is administered alone and in combination with Ganfeborole in healthy female participants of non-childbearing potential.
Trial Details
NCT Number NCT07784894
Lead Sponsor GlaxoSmithKline
Collaborators: UNITE4TB consortium
Conditions Tuberculosis
Enrollment 28 participants
Start Date 2026-09-01
Primary Completion 2026-11-24 (estimated)
Study Completion 2026-11-24 (estimated)
Updated on ClinicalTrials.gov 2026-08-25