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)

Trial Profile

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)

Planning
Phase of Trial: Phase I

Latest Information Update: 11 Oct 2017

At a glance

  • Drugs ABI 1968 (Primary)
  • Indications Cervical intraepithelial neoplasia
  • Focus Adverse reactions
  • Sponsors Antiva Biosciences
  • Most Recent Events

    • 06 Oct 2017 Planned initiation date changed from 1 Sep 2017 to 1 Oct 2017.
    • 31 Mar 2017 New trial record
    • 28 Mar 2017 According to an Antiva Biosciences media release, this trial is expected to commence later in 2017.
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