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Brief Title: Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Official Title: Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Study ID: NCT03202992
Brief Summary: This study evaluates the use of ABI-1968, a topical cream, in the treatment of anal precancerous lesions in adults with and without human immunodeficiency virus (HIV) infection.
Detailed Description:
Minimum Age: 27 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Center, San Francisco, California, United States
Research Center, Orlando, Florida, United States
Research Center, Chicago, Illinois, United States
Research Center, New York, New York, United States
Research Center, Winston-Salem, North Carolina, United States
Research Center, Sydney, Darlinghurst, Australia
Name: Clinical Operations
Affiliation: Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may use the contacts provided below.
Role: STUDY_CHAIR