Asthma
Conditions
Brief summary
This study is a multi-center, randomized, double-blind, placebo-controlled Phase II clinical study to evaluate the efficacy, safety, PK characteristics, PD effects and immunogenicity of CM310 in subjects with moderate to severe asthma. The study consists of three periods, including an up to 4-week screening period, a 24-week randomized treatment period, and a 8-week safety follow-up period.
Interventions
DRUGCM310
CM310 Recombinant Humanized Monoclonal Antibody Injection
OTHERPlacebo
Placebo
Sponsors
Keymed Biosciences Co.Ltd
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Subjects are able to understand the nature of the study and voluntarily sign the ICF. * Diagnosed with asthma according to the 2021 version of the GINA guidelines for at least 1 year. * Pre-bronchodilator FEV1 measurement ≤ 80% of predicted normal value. * Subjects must have experienced a severe asthma exacerbation within 12 months prior to screening, and have not experienced a severe asthma exacerbation within 1 month prior to screening.
Exclusion criteria
* Women of childbearing potential have a positive pregnancy test result during the screening period; women who are pregnant or lactating. * Received biologics with the same therapeutic purpose within 6 months prior to screening, such as similar IL-4Rα antagonist, IL-5/5R, anti-IgE monoclonal antibody (mAb). * Diagnosed with chronic obstructive pulmonary disease (COPD) or other lung disorders that may compromise lung function (including but not limited to idiopathic pulmonary fibrosis, allergic granulomatous angiitis, bronchopulmonary aspergillosis allergic, pulmonary tuberculosis, etc.).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in pre-bronchodilator FEV1 (forced expiratory volume in 1 second) at 12 weeks. | 12 weeks | Absolute change from baseline in pre-bronchodilator FEV1 in each dose group at 12 weeks of CM310 treatment compared with placebo. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percent change from baseline in pre-bronchodilator FEV1 at each evaluation time point. | 24 weeks | Percent change from baseline in pre-bronchodilator FEV1 at each evaluation time point. |
| Annualized rate of subjects experiencing severe asthma exacerbations. | 24 weeks | Annualized rate of subjects experiencing severe asthma exacerbations during the 24-week randomized treatment period. |
| Time to the first onset of the severe asthma exacerbation event. | 24 weeks | Time from baseline to the first onset of the severe asthma exacerbation event. |
| Annualized rate of subjects experiencing the event of loss of asthma control (LOAC). | 24 weeks | Annualized rate of subjects experiencing the event of loss of asthma control (LOAC) during the 24-week randomized treatment period. |
| Time to the onset of the first event of LOAC. | 24 weeks | Time from baseline to the onset of the first event of LOAC. |
| FEV1 percentage of predicted value (FEV1% Pred) | 32 weeks | FEV1 percentage of predicted value (FEV1% Pred) |
| Peak diurnal and nocturnal expiratory flow (PEF) | 32 weeks | Peak diurnal and nocturnal expiratory flow (PEF) |
| Forced vital capacity (FVC) | 32 weeks | Forced vital capacity (FVC) |
| Maximal mid-expiratory flow (MMEF) | 32 weeks | Maximal mid-expiratory flow (MMEF) |
| Change from baseline in pre-bronchodilator FEV1 at each evaluation time point. | 24 weeks | Absolute change from baseline in pre-bronchodilator FEV1 at each evaluation time point. |
| Change from baseline in the Asthma Control Questionnaire-5 (ACQ-5) score at each evaluation time point. | 32 weeks | The ACQ-5 is a questionnaire used to evaluate the degree of asthma control. Each question is scored from 0 to 6 (on a 7-point scale) according to its severity. The higher the score, the less satisfactory symptom control is. |
| Change from baseline in asthma symptom score at each evaluation time point. | 32 weeks | Patients will record total symptom scores in morning（a 0-4 scale, with 0=no symptoms, 4=inability to fall asleep at night due to symptoms) and afternoon (a 0-5 scale, with 0=no symptoms, 5=severe symptoms, unable to work or perform daily activities). |
| Incidence of Adverse events (AEs) | 32 weeks | Incidence of AEs, including any abnormal physical examinations, abnormal vital signs, abnormal ECG, and abnormal lab testing. |
| Trough concentration at steady-state of CM310 | 32 weeks | To evaluate the trough concentration at steady-state of CM310 for each dose group. Population pharmacokinetic analysis is performed using a nonlinear mixed-effects model. |
| Human thymus and activation-regulated chemokine (TARC) | 32 weeks | Change from baseline in TARC at each evaluation time point for each dose group. |
| Fractional exhaled nitric oxide (FeNO). | 32 weeks | Change from baseline in FeNO at each evaluation time point for each dose group. |
| Total IgE (immunoglobulin E) | 32 weeks | Change from baseline in total IgE at each evaluation time point for each dose group. |
| Anti-drug antibodies (ADAs) and neutralizing antibodies (Nabs). | 32 weeks | Incidence of anti-drug antibodies (ADAs) and neutralizing antibodies (Nabs) (if applicable). |
| Change from baseline of FEV1 after the use of bronchodilator. | 32 weeks | Change from baseline of FEV1 after the use of bronchodilator. |
Countries
China
Outcome results
None listed