Clinical trial
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
NCT03239223 is registered in ClinicalTrials.gov with Antiva Biosciences as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
- Lead sponsor
- Antiva Biosciences
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- January 1, 2018
- Completion date
- October 30, 2018
- Enrollment
- 16 (actual)
- Sites
- 9
Conditions
As the registry lists them; a condition with its own page is linked.
cervical cancer, cervical dysplasia, cervical intraepithelial neoplasia, cervical neoplasm, cin, high-grade cervical intraepithelial neoplasia, high-grade squamous intraepithelial lesions, hsil, hsil of cervix, human papilloma virus