← Eichor
Study identifier: NCT06075264 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Phase II Study of Artesunate Ointment for the Treatment of Vulvar High Grade Squamous Intraepithelial Lesions (Vulvar HSIL, VIN2/3)

Condition: Vulvar Diseases · HPV Infection · Vulvar HSIL  ·  Sponsor: Frantz Viral Therapeutics, LLC

PhasePhase 2
Planned participants27
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a phase II double-blind, placebo-controlled study of artesunate ointment for the treatment of HPV-associated vulvar HSIL (usual type vulvar intraepithelial neoplasia 2/3).

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

Talk to the study team

Mihaela Plesa  ·  440-255-1155  ·  fvtinfo@frantzgroup.com

Ahmad Bayat, MD  ·  301-956-2523

Always discuss trial participation with your own doctor first.

Locations (5)

Florida Gynecologic OncologyFort Myers, Florida, United StatesRecruiting
Ascension St. VincentIndianapolis, Indiana, United StatesRecruiting
Cleveland Clinic Fairview HospitalCleveland, Ohio, United StatesRecruiting
Cleveland Clinic FoundationCleveland, Ohio, United StatesRecruiting
Hillcrest HospitalMayfield Heights, Ohio, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06075264