A randomized, Double-blind, Placebo-controlled, Single and Multiple Dose Escalation Study in Healthy Participants to Evaluate Safety, Tolerability and Pharmacokinetics of ABI-2280 Vaginal Gel and Tablet as Applied to the Cervix
Latest Information Update: 11 Mar 2022
At a glance
- Drugs ABI-2280 (Primary)
- Indications Cervical intraepithelial neoplasia
- Focus Adverse reactions
- Sponsors Antiva Biosciences
Most Recent Events
- 10 Mar 2022 Planned number of patients changed from 72 to 48.
- 10 Mar 2022 Planned End Date changed from 30 Mar 2022 to 3 Jul 2022.
- 06 Jan 2022 Status changed from not yet recruiting to recruiting, according to an Antiva Biosciences media release.