A Randomized, Double-blind, Placebo-controlled Phase II Clinical Study Evaluating the Efficacy and Safety of CM512 Injection in Subjects With Moderate-to-severe Asthma.

Status: Recruiting
Location: See location...
Intervention Type: Drug, Biological
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
China
The First Clinical Hospital of Guangzhou Medical University
RECRUITING
Guangzhou
Contact Information
Primary
Qian Jia
qianjia@keymedbio.com
028-88610620
Time Frame
Start Date: 2025-08-19
Estimated Completion Date: 2027-07-21
Participants
Target number of participants: 200
Treatments
Experimental: Group 1
Placebo_comparator: Group 2
Related Therapeutic Areas
Sponsors
Leads: Keymed Biosciences Co.Ltd

This content was sourced from clinicaltrials.gov

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