Subcutaneously CM310/Placebo in Patients With Moderate-to-Severe Atopic Dermatitis (AD)
Launched by KEYMED BIOSCIENCES CO.LTD · Mar 17, 2021
Trial Information
Current as of July 21, 2025
Completed
Keywords
ClinConnect Summary
Subjects will be required to apply moisturizers after ICF signed and continue throughout the study.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Diagnosed as AD for at least 12 months before Screening, with below requirements: 1)EASI score ≥16 at Screening and Baseline; 2) IGA score ≥3 (0-5 points scale) at Screening and Baseline; 3) ≥10% BSA of AD involvement at Screening and Baseline; 4) Pruritus NRS average score ≥3 at Baseline.
- • Inadequate response to topical medications.
- Exclusion Criteria:
- • Not enough washing-out period for previous therapy.
- • Concurrent disease/status which may potentially affect the efficacy/safety judgement.
- • Organ dysfunction.
- • pregnancy.
- • Other.
About Keymed Biosciences Co.Ltd
Keymed Biosciences Co., Ltd. is a leading biotechnology firm dedicated to the development of innovative therapeutic solutions, particularly in the fields of oncology and autoimmune diseases. With a strong emphasis on research and development, Keymed leverages cutting-edge technologies and a highly skilled team to advance its pipeline of novel biologics and small molecule drugs. The company is committed to improving patient outcomes through rigorous clinical trials and a robust regulatory strategy, aiming to deliver safe and effective treatments to address unmet medical needs globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chengdu, Sichuan, China
Yantai, Shandong, China
Beijing, Beijing, China
Beijing, Beijing, China
Changsha, Hunan, China
Hangzhou, Zhejiang, China
Jinan, Shandong, China
Beijing, Beijing, China
Hangzhou, Zhejiang, China
Zhenjiang, Jiangsu, China
Qingdao, Shandong, China
Changchun, Jilin, China
Taiyuan, Shanxi, China
Beijing, Beijing, China
Changsha, Hunan, China
Hangzhou, Zhejiang, China
Guangzhou, Guangdong, China
Beijing, Beijing, China
Chongqing, Chongqing, China
Wuxi, Jiangsu, China
Changchun, Jilin, China
Jinan, Shandong, China
Shanghai, Shanghai, China
Tianjin, Tianjin, China
Hangzhou, Zhejiang, China
Ningbo, Zhejiang, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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