Study of CM512 Injection in Subjects With Moderate-to-severe Asthma
Recruiting · NCT07011524 · Interventional (participants receive a specific treatment) · Lead sponsor: Keymed Biosciences Co.Ltd
View the official record on ClinicalTrials.gov →Interventions studied
CM512 injectionPlacebo
What this trial is about
This study is a multicenter, randomized, double-blind, placebo-controlled phase II clinical trial evaluating the efficacy, safety, pharmacokinetics, pharmacodynamics, and immunogenicity of CM512 in subjects with moderate-to-severe asthma.
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
- Able to understand and comply with procedures of the protocol, and voluntarily sign the Informed Consent Form.
- Age ≥ 18 years old and ≤ 75 years old.
- Body mass index (BMI) ≥ 18.0 kg/(m\*m).
- Documented treatment with medium to high dose Inhaled Corticosteroids (ICS) in combination with asthma controller medication for at least 3 months with a stable dose ≥1 month prior to Visit 1.
- Documented history of at least 1 severe asthma exacerbation events within 12 months, and at least one of the exacerbations should occur during the treatment of medium-to-high dose ICS.
- Asthma Control Questionnaire-6 (ACQ-6) score ≥1.5
Exclusion criteria
- Women of childbearing potential have a positive pregnancy test result during the screening period; women who are pregnant or lactating.
- With a history of drug abuse within the past 5 years before screening visit.
- Allergic or intolerant to CM512 injection or placebo components, or with a history of severe drug allergies or anaphylactic shock.
- With any medical or non-medical conditions that are not suitable for participation in this study by investigators.
Where it is running
1 location listed.
- The First Clinical Hospital of Guangzhou Medical University - Guangzhou, Guangdong, China