Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis (IPF) is a rare lung disease characterized by the gradual scarring of lung tissue, which makes it increasingly difficult to breathe over time.
We are assessing the safety and tolerability of CMR316 in healthy volunteers and patients with Idiopathic Pulmonary Fibrosis. This study aims to understand how well the treatment is tolerated.
Health conditions and diseases that the clinical trial is designed to study and treat.
Idiopathic Pulmonary Fibrosis (IPF) is a rare lung disease characterized by the gradual scarring of lung tissue, which makes it increasingly difficult to breathe over time.
Locations and medical facilities where this clinical trial is currently recruiting or conducting research. Select the locations where you would like to participate.
Disclaimer: Parts of this content have been automatically extracted from the EU Clinical Trials registry. While we strive for accuracy, please always contact the trial site or sponsor directly for correct and official information before making any decisions about participation. View on EU Clinical Trials.