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Study identifier: NCT07683806 Synced from ClinicalTrials.gov · August 05, 2026
● Not Yet Recruiting

Efficacy and Safety of Roflumilast Foam 0.3% in Trial Participants With Seborrheic Dermatitis

Condition: Seborrheic Dermatitis  ·  Sponsor: Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.

PhasePhase 3
Planned participants309
Who can joinAll sexes, 9 Years to no upper limit
Healthy volunteersNo

About this study

This study will assess the safety and efficacy of Roflumilast foam 0.3% (ZORYVE®) versus vehicle applied once a day for 8 weeks by trial participants with seborrheic dermatitis.

This description comes directly from the study's public registry record.

Talk to the study team

Huadong Medicine  ·  +86-0571-89918267  ·  cxyguweizhi@eastchinapharm.com

Always discuss trial participation with your own doctor first.

Locations (44)

The First Affiliated Hospital of Wannan Medical HospitalWuhu, Anhui, China
The Second Affiliated Hospital of Wannan Medical HospitalWuhu, Anhui, China
The first affilated hospital of Fujian Medical universityFuzhou, Fujian, China
The Second Affiliated Hospital of Xiamen Medical CollegeXiamen, Fujian, China
Dermatology Hospital of Southern Medical UniversityGuangzhou, Guangdong, China
Shenzhen Children's HospitalShenzhen, Guangdong, China
Hainan Fifth People's HospitalHaikou, Hainan, China
Beijing Children's Hospital, Capital Medical University Baoding HospitalBaoding, Hebei, China
The Second Affiliated Hospital of Harbin Medical UniversityHarbin, Heilongjiang, China
The Second Affiliated Hospital of Henan University of science and technologyLuoyang, Henan, China
Nanyang Central HospitalNanyang, Henan, China
Sanmenxia Central HospitalSanmenxia, Henan, China

+ 32 more locations — full list on the registry record.

Sponsor or site team? See the site landscape for this trial — listed sites, countries, and recruiting-density context.

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