A Phase 2 Randomized Double-blind Placebo-controlled Repeat-dose Study of KB001-A in Subjects with Cystic Fibrosis Infected with Pseudomonas aeruginosa
Study on the Safety and Effectiveness of an Investigational Medication for Cystic Fibrosis with Chronic Pseudomonas Infection
Brief description of study.
The purpose of this study is to determine if multiple doses of KB001-A are safe and effective in people with Cystic Fibrosis and chronic Pseudomonas infection.
Detailed description of study
The purpose of this study is to determine if multiple doses of KB001-A are safe and effective in people with Cystic Fibrosis and chronic Pseudomonas infection.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Cystic Fibrosis
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Age: 12 years - 50 years
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Gender: All
This study investigates the safety and effectiveness of an investigational medication in people with Cystic Fibrosis who have a chronic Pseudomonas infection. Cystic Fibrosis is a genetic disorder that affects the lungs and digestive system. Pseudomonas is a type of bacteria that can cause lung infections in people with Cystic Fibrosis.
Participants in the study will receive multiple doses of the investigational medication. The study will include procedures to monitor the safety and effectiveness of the treatment, which might involve regular check-ups and tests to assess lung function and infection levels.
- Who can participate: Participants must meet age criteria and key eligibility factors, which will be specified by the study.
- Study details: Participants will receive multiple doses of an investigational medication. Regular monitoring will be conducted to evaluate the treatment's impact on lung function and infection.
Interested in the study?
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