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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)

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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)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 03 Oct 2021

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At a glance

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

Most Recent Events

  • 15 Nov 2018 Status changed from active, no longer recruiting to completed.
  • 01 Oct 2018 Planned primary completion date changed from 1 Sep 2018 to 30 Oct 2018.
  • 07 Aug 2018 Status changed from recruiting to active, no longer recruiting.

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