This study is currently not recruiting participants.

A Phase III randomized double-blind placebo-controlled study of AeroVanc for the treatment of persistent methicillin-resistant Staphylococcus aureus lung infection in cystic fibrosis patients

Study of Investigational Medication for CF with MRSA Lung Infection

Not Recruiting
100 years or below
All
Phase N/A
1 Location

Brief description of study.

The purpose of this study is to evaluate the effectiveness and safety of AeroVanc compared to placebo in patients with CF and a chronic MRSA lung infection.

Detailed description of study

The purpose of this study is to evaluate the effectiveness and safety of AeroVanc compared to placebo in patients with CF and a chronic MRSA lung infection.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: cystic fibrosis,MRSA
  • Age: 100 years or below
  • Gender: All

The purpose of this study is to evaluate the effectiveness and safety of an investigational medication compared to a placebo in patients with cystic fibrosis (CF) who have a chronic lung infection caused by methicillin-resistant Staphylococcus aureus (MRSA). Cystic fibrosis is a genetic condition that affects the lungs and makes it difficult to breathe due to thick, sticky mucus. MRSA is a type of bacteria that is resistant to many antibiotics, making infections hard to treat.

Participants in the study will be randomly assigned to one of two study arms. One group will receive the investigational medication, while the other group will receive a placebo, which is an inactive substance that looks like the investigational medication but does not contain any medicine. The study will compare the effects of the investigational medication and the placebo on lung function and overall health.

  • Who can participate: This study is open to individuals aged 18 and older diagnosed with cystic fibrosis who have a chronic MRSA lung infection. Participants must meet specific health criteria related to their condition.
  • Study details: Participants will be randomly assigned to receive either the investigational medication or a placebo. A placebo is an inactive substance that looks like the investigational medicine but does not contain any medicine.
Updated on 19 Feb 2024. Study ID: 1708793689

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