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A Safety and Efficacy Study to Evaluate Rosacea

Papulopustular Rosacea Clinical Trial

Official title:
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

Clinical Trial Summary

To evaluate the safety, efficacy, and pharmacokinetic profile of ascending concentrations of the study medication compared with vehicle in subjects with rosacea.

Clinical Trial Description

This is primarily a safety study to evaluate the safety of AIV001 when administered to subjects with rosacea. Exploratory efficacy measures will also be collected as well as pharmacokinetic profiles. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03883945
Study type Interventional
Source AiViva BioPharma, Inc.
Contact
Status Withdrawn
Phase Phase 1/Phase 2
Start date July 2021
Completion date August 2022
View Details
See also
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