By participating in our study and sharing your DNA, you will help us to identify the genetic markers of the disease and lead to earlier identification and treatment for your family members who may be at risk and people with IPF around the world.
You are eligible to participate if you have IPF or if you have family members with the disease. By comparing your DNA with thousands of other participants we can start to identify the markers of the disease. Your participation can help lead to early diagnosis and a cure for Idiopathic Pulmonary Fibrosis.
Contact us today to sign up for the study!
We need your help. Just think, how do we find early disease that is undiagnosed and not manifesting any signs or symptoms? The answer is to find individuals at higher risk for IPF and screen them for early disease. At the same time, we need to collect blood samples. These higher-risk individuals are the siblings or children of those with IPF that have on or more of the high-risk genetic variants. Therefore, if you or someone in your family has IPF, we need to study your family members to identify pre-clinical IPF.
Have questions? Feel free to contact our research coordinators for more details.
12631 E 17th Ave
Aurora, CO, USA 80045