Comparison of Efficacy and Safety of Azelaic Acid 15% Gel With Its Vehicle in Subjects With Mild to Moderate Acne
A 12-week, Randomized, Double-blind, Multicenter Study Comparing the Clinical Efficacy and Safety of Azelaic Acid 15% Gel (SH H 655 BA) With Its Vehicle (SH H 655 PBA) in Patients With Mild to Moderate Acne.
Sponsor: Bayer
A PHASE3 clinical study on Acne Vulgaris, this trial is completed. The trial is conducted by Bayer and has accumulated 8 data snapshots since 2002. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Change History
8 versions recorded-
Sep 2024 — Present [monthly]
Completed PHASE3
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Jul 2024 — Sep 2024 [monthly]
Completed PHASE3
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Jul 2023 — Jul 2024 [monthly]
Completed PHASE3
-
Jan 2021 — Jul 2023 [monthly]
Completed PHASE3
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May 2020 — Jan 2021 [monthly]
Completed PHASE3
▶ Show 3 earlier versions
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Jun 2018 — May 2020 [monthly]
Completed PHASE3
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Feb 2017 — Jun 2018 [monthly]
Completed PHASE3
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE3
First recorded
Jan 2002
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Bayer
- LEO Pharma
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
Albuquerque, United States, Bay Shore, United States, Boulder, United States, Bryan, United States, Cincinnati, United States, Hershey, United States, Knoxville, United States, Lexington, United States, Mobile, United States, Newnan, United States and 6 more location s