Study of CM310 Injection in Subjects With Moderate-to-Severe Atopic Dermatitis
Launched by KEYMED BIOSCIENCES CO.LTD · Jan 27, 2023
Trial Information
Current as of July 21, 2025
Completed
Keywords
ClinConnect Summary
This study includes screening, treatment and follow-up periods. 160 subjects will be enrolled to receive CM310.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Have the ability to understand the study and voluntarily sign a written ICF.
- • Age ≥ 18 and ≤ 75 years old, male or female.
- • The fertile subjects agreed to take effective contraceptive measures throughout the study period.
- • The subjects can communicate well with the investigators and complete the follow-up according to the protocol.
- Exclusion Criteria:
- • Live vaccine or attenuated live vaccine has been vaccinated or planned to be vaccinated within 12 weeks before randomization.
- • He received allergen-specific immunotherapy (desensitization therapy) within 6 months before randomization.
- • Major surgery is planned during the study period.
- • Previous history of atopic keratoconjunctivitis and corneal involvement.
- • Other combined skin diseases that may affect the evaluation of the study.
- • Confronting IL-4R α Monoclonal antibody or CM310/placebo drug or ingredient allergy.
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
Hangzhou, Zhejiang, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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