This study evaluates the use of ABI-1968, a topical cream, in the treatment of cervical precancerous lesions in females without human immunodeficiency virus (HIV) infection.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
8
Multiple Doses of Topical ABI-1968 Cream with 4 once weekly doses administered in up to 5 Cohorts
Research Center
Bloemfontein, Free State, South Africa
Safety & Tolerability of ABI-1968 for the treatment of cHSIL
Number of Adverse Events related to treatment
Time frame: 42 days
Systemic exposure to ABI-1968 Topical Cream following topical application to the cervix.
Plasma concentrations of ABI-1968 over time
Time frame: 42 days
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