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โ† Trials
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Efficacy and Safety Study of 610 in Patients With Severe Asthma

RecruitingPhase 3Ages 18 Years - 75 YearsAllSunshine Guojian Pharmaceutical (Shanghai) Co., Lโ€ฆ
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In plain words

What the trial is, and whether it could suit you

The primary objective of the study is to evaluate the efficacy and safety of 610 in Chinese adults with severe asthma.

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. Able to give written informed consent prior to participation in the study. 2. Male or female adults ages 18 to 75 years old when signing the informed consent. 3. Documented diagnosis of asthma for at least one year prior to screening. 4. History of physician-diagnosed asthma requiring treatment with ICS and at least one other control medication for at least 6 months prior to screening. Exclusion Criteria: 1. Presence of a known pre-existing, clinically important lung condition other than asthma. 2. Severe asthma exacerbation within 4 weeks prior to randomization. 3. Subjects with any eosinophilic diseases other than asthma. 4. Known, pre-existing severe or clinically significant cardiovascular disease. 5. known, pre-existing other concurrent clinically significant medical conditions that are uncontrolled with standard treatment. 6. Subjects who have active Hepatitis B, Hepatitis C or HIV infections as determined by positive results at Screening. 7. Subjects with allergy/intolerance to a monoclonal antibody.
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What it tests

  • 610
  • Placebo
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Where

1 site
Shanghai General Hospital
Shanghai, China
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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