A Randomized, Double-Blind, Vehicle-Controlled, Parallel-Group, Dose-Escalation Study to Evaluate the Safety and Pharmacokinetics of Intradermally Administered AIV001 in Subjects With Papulopustular Rosacea

Status: Withdrawn prior to enrolment

Phase of Trial: Phase I/II

Latest Information Update: 20 May 2022

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At a glance

Drugs AIV 001 (Primary)
Indications Erythema; Rosacea
Focus Adverse reactions
Sponsors AiViva BioPharma

Most Recent Events

11 May 2022 Status changed from not yet recruiting to withdrawn prior to enrolment.
11 Jan 2021 Planned End Date changed from 1 Mar 2022 to 1 Aug 2022.
11 Jan 2021 Planned primary completion date changed from 1 Dec 2021 to 1 Jul 2022.

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