A Study to Investigate the Efficacy and Safety of SHR-1905 in Patients With Moderate-to-severe Atopic Dermatitis
Recruiting · NCT07211542 · Interventional (participants receive a specific treatment) · Lead sponsor: Guangdong Hengrui Pharmaceutical Co., Ltd
View the official record on ClinicalTrials.gov →Interventions studied
SHR-1905 InjectionSHR-1905 Injection Blank Preparation
What this trial is about
This trial was designed to evaluate the efficacy and safety of SHR-1905 in patients with moderate-to-severe atopic dermatitis.
Who can take part
Age range
18 Years to 75 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 2
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- The subjects have voluntarily signed the informed consent form prior to the start of any procedures related to the study, are able to communicate smoothly with the researcher, understand and are willing to strictly abide by the requirements of this clinical research protocol to complete the study.
- At the time of signing the informed consent, the subjects are ≥ 18 years old and ≤ 75 years old, male or female.
- Have atopic dermatitis at screening.
Exclusion criteria
- Hypersensitivity to the study drug or any ingredient in the study drug.
- Have other active skin disease or skin complications due to other conditions that may affect the evaluation of Atopic Dermatitis (AD).
- Has malignancy or has a history of malignancy.
- Have serious concomitant diseases and other conditions that the investigator considers inappropriate to participate in this trial.
- Females who are pregnant or lactating.
Where it is running
1 location listed.
- Dermatology Hospital of Southern Medical University - Guangzhou, Guangdong, China