Status:

UNKNOWN

The Study of CM326 in Patients With Moderate-to-severe Atopic Dermatitis

Lead Sponsor:

Keymed Biosciences Co.Ltd

Conditions:

Moderate-to-severe Atopic Dermatitis

Eligibility:

All Genders

18-70 years

Phase:

PHASE1

PHASE2

Brief Summary

This is a multi-center, randomized, double blind, placebo-controlled multiple dose escalation study to evaluate the safety, tolerance, PK, PD, immunogenicity and preliminary efficacy of CM326 in moder...

Detailed Description

The study consists of 3 periods, a up-to-4-week Screening Period, a 12-week randomized Treatment Period and a 12-week Safety Follow-up Period.

Eligibility Criteria

Inclusion

  • With confirmed Atopic Dermatitis (AD) at least 12 months before the screening
  • Eczema Area and Severity Index (EASI) score ≥16 at screening and baseline
  • Investigator's Global Assessment (IGA) score ≥3 at screening and baseline
  • Body Surface Area (BSA) of involvement of atopic dermatitis ≥10% at screening and baseline
  • The weekly mean score of daily peaks in pruritus NRS at baseline ≥4
  • Provide signed informed consent

Exclusion

  • Not enough washing-out period for previous therapy.
  • Presence of other concomitant and poorly controlled serious diseases or recurrent chronic diseases, including but not limited to active infections, cardiovascular and cerebrovascular diseases, pulmonary tuberculosis or other pathogen infections, diabetes mellitus, autoimmune diseases, human immunodeficiency virus (HIV) infection, active hepatitis B, hepatitis C or parasitosis, neoplasm malignant, etc.
  • Patients with severe hepatic or renal impairment, characterized by aspartate aminotransferase (AST) or alanine aminotransferase (ALT) level \> 2 times of upper limit of normal (ULN), total bilirubin \>1.5 times of upper limit of normal (ULN) or serum creatinine level \> upper limit of normal (ULN).
  • Womens who are pregnant or breastfeeding, or who plan to become pregnant during the study.

Key Trial Info

Start Date :

February 17 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2023

Estimated Enrollment :

54 Patients enrolled

Trial Details

Trial ID

NCT05186922

Start Date

February 17 2022

End Date

January 1 2023

Last Update

March 9 2022

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Peking University People's hospital

Beijing, Beijing Municipality, China