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Spots Global Cancer Trial Database for A Study of ABI-2280 Vaginal Tablet in Participants With Cervical Intraepithelial Neoplasia

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Trial Identification

Brief Title: A Study of ABI-2280 Vaginal Tablet in Participants With Cervical Intraepithelial Neoplasia

Official Title: An Open-Label Single and Multiple-dose, Study to Evaluate Safety, Tolerability and Efficacy of ABI-2280 Vaginal Tablet in Participants With Cervical Squamous Intraepithelial Lesions

Study ID: NCT05502367

Interventions

ABI-2280

Study Description

Brief Summary: This is an open-label study to evaluate the safety, tolerability, and efficacy of ABI-2280 in participants with cervical squamous intraepithelial lesions. This study is divided into 2 parts - Part A and Part B. Part A consists of 3 dose escalating cohorts. Part B is a dose expansion cohort. Participants will self-administer ABI-2280.

Detailed Description:

Keywords

Eligibility

Minimum Age: 25 Years

Eligible Ages: ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

East Sydney Doctors, Darlinghurst, New South Wales, Australia

Gold Coast University Hospital, Southport, Queensland, Australia

Farmvos, Bloemfontein, Free State, South Africa

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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