Acne Vulgaris Clinical Trial
Official title:
Multicenter, Double-blind, Double-dummy, Randomized Parallel Group Study to Evaluate the Safety and Efficacy of SH D 00659 E for 6 Treatment Cycles in Female Patients With Acne Papulopustulosa in Comparison to SH D 00659 G and Placebo.
The purpose of the study is to determine safety and efficacy of an oral contraceptive in treating acne papulopustulosa.
The study has previously been posted by Schering AG, Germany. Schering AG, Germany has been renamed to Bayer Schering Pharma AG, Germany.Bayer Schering Pharma AG, Germany is the sponsor of the trial. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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Bio-equivalence Study With Clinical Endpoints in the Treatment of Acne Vulgaris
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Phase 1 | |
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Phase 3 | |
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N/A | |
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Phase 3 | |
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N/A | |
| Not yet recruiting |
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Phase 2 | |
| Not yet recruiting |
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A Study Comparing the Efficacy and Safety of IDP-121 and IDP-121 Vehicle Lotion in the Treatment of Acne Vulgaris
|
Phase 3 | |
| Completed |
NCT02709902 -
Study Comparing Adapalene/BP Gel to EPIDUO® FORTE and Both to a Placebo Control in Treatment of Acne Vulgaris
|
Phase 1 | |
| Not yet recruiting |
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A Study Comparing the Efficacy and Safety of IDP-121 and IDP-121 Vehicle Lotion in the Treatment of Acne Vulgaris
|
Phase 3 | |
| Completed |
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Phase 1 | |
| Completed |
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N/A | |
| Completed |
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Phase 1 | |
| Completed |
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Phase 1 | |
| Completed |
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N/A | |
| Completed |
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|
Phase 2 | |
| Completed |
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Phase 4 | |
| Completed |
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Phase 4 |