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Study identifier: NCT07514416 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

To Test a New Drug (LCFA-01) for Safety and PK in Healthy Adults for Bacterial Vaginosis Infection.

Condition: Bacterial Vaginosis Treatment  ·  Sponsor: Massachusetts General Hospital

PhasePhase 1
Planned participants30
Who can joinFemale, 18 Years to 40 Years
Healthy volunteersYes

About this study

This study is being done to check how safe and comfortable LCFA-01 is when used inside the vagina. LCFA-01 is a natural product that contains oleic acid, and it comes as a soft gel capsule that participants will place in the vagina using their fingers. The main purpose of the study is to make sure the product is safe and does not cause any problems or discomfort. The study will also measure how much of the product stays in the vagina and whether any of it enters the bloodstream. This helps researchers understand how the body absorbs and handles the product. Finally, the study will also look at early signs of how the product might affect the natural bacteria in the vagina. In the future, LCFA-01 may be used to treat bacterial vaginosis (BV).

This description comes directly from the study's public registry record.

Talk to the study team

Dr Douglas Kwon  ·  +18572687160  ·  dkwon@mgh.harvard.edu

Dr Caroline Mitchell, MD, MPH  ·  +16177242182  ·  caroline.mitchell@mgh.harvard.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Allied Health Hub MorayfieldBrisbane, Queensland, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT07514416