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Clinical Trial Summary

The study evaluated the safety, tolerability, and efficacy of ACCU-D1 when applied twice daily for 12 weeks in adult participants with moderate to severe acne rosacea. Two-third of the participants received ACCU-D1 while one-third of the participants received vehicle control.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03064438
Study type Interventional
Source Accuitis, Inc.
Contact
Status Completed
Phase Phase 2
Start date November 28, 2017
Completion date June 18, 2018

See also
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Completed NCT04555525 - A Pilot Study on the Use of Seysara for Rosacea Phase 4