Pulmonary Arterial Hypertension
Pulmonary Arterial Hypertension (PAH) is a rare but serious condition characterized by high blood pressure in the arteries of the lungs, leading to symptoms such as shortness of breath, fatigue, and chest pain.
We are studying a new treatment called LTP001 in healthy adults and in individuals with pulmonary arterial hypertension. The goal is to evaluate its safety and how well it may improve exercise capacity and overall health.
Health conditions and diseases that the clinical trial is designed to study and treat.
Pulmonary Arterial Hypertension (PAH) is a rare but serious condition characterized by high blood pressure in the arteries of the lungs, leading to symptoms such as shortness of breath, fatigue, and chest pain.
These questions help us understand your situation so we can let the trial team know whether you might be a potential match. This is not a medical evaluation and is not part of the official screening, the study doctor will make the final decision..
Experimental substances that are being investigated in this clinical trial. These are not yet approved for general use.
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.