Overview
The purpose of this study is to evaluate the Pharmacodynamic, Efficacy and Safety of SHR-1703 in Asthma Patients with Eosinophil Phenotype
Eligibility
Inclusion Criteria:
- At least 12 years of age
- A minimum weight of 40kg
- A medical history of at least 1 year that meets the diagnosis of asthma;
- Current treatment with medium- or high- doses of ICS for at least 6 months and using steadily at least 3 months
- Current treatment with an additional controller medication, besides ICS, for at least 3 months and using steadily at least 1 month
- Absolute count of blood eosinophils suggests eosinophilic asthma
- During the screening period and baseline, pre- BD FEV1% < 80%
- During the screening period and baseline, ACQ-6 score indicates asthma poor control
- History of severe asthma exacerbation within the past 12 months prior to screening
- Good compliance with eDiary completion
- Take efficient contraceptive measures
- Voluntarily sign the informed consent form to participate in this study
Exclusion Criteria:
- With other condition that could lead to elevated eosinophils
- With Clinically significant pulmonary diseases
- With existing immunodeficiency disease
- With other clinically significant diseases that may affect lung function
- With uncontrolled severe cardiovascular and cerebrovascular diseases
- With uncontrolled hypertension and/or diabetes
- With exacerbation, allergic rhinitis or sinusitis attacks, or clinical significant infection requiring intervention during 4 weeks prior to randomization
- Recent major surgeries or surgical plans during the study period, or treatment measures that investigators believe may affect subject evaluation
- Existing parasitic infections
- Diagnosed as malignant tumor within the first 5 years of randomization
- Significant abnormalities in screening period or baseline laboratory tests
- Screening period or baseline ECG QTc prolongation
- Prohibited drugs using during the pre randomization period
- Participated in other clinical trials within 30 days prior to screening and used research drugs containing active ingredients, or was still within 5 half lives of the research drug at the time of screening
- Smoking or quitting smoking for less than 6 months during screening, or previous smoking history ≥ 10 pack years
- History of drug use, alcoholism, or substance abuse within the past year prior to screening
- Allergic or intolerant to IL-5 monoclonal antibodies or other biological agents
- Pregnant or lactating subjects
- Other reasons why the researcher deemed it unsuitable for conducting this experiment