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Search / Trial NCT04805411

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

Atopic Dermatitis

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.

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

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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