Studies open frequently. If interested in the latest information regarding our studies, please call Thelma Harrington, RRT, MS, MBA 410-328-1473.

Pulmonary Rehab for IPF Patients

Principal Investigator; Edward J Britt, MD 

If you have Idiopathic Pulmonary Fibrosis (IPF) and are taking Ofev®, learn about this research study evaluating pulmonary rehabilitation (PR), a program that includes exercise, education, and support to improve the health of IPF patients.

Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. It works by blocking the action of certain natural chemicals in your body (such as epinephrine) that affect the heart and blood vessels. This lowers heart rate, blood pressure, and strain on the heart. This research study will test how well once daily metoprolol succinate works to reduce COPD flare-ups.

  • Eligibility:40+ years old; IPF diagnosis in the past 5 years
  • Reimbursements: In addition to travel and transport costs, you will be paid up to a total of $600 if you complete this study up to Week 52. For every on-site visit completed after Week 52 you will be paid $50.
  • Contact: Call 410-328-1473 or email
  • STUDY STATUS: Enrolling


Principal Investigator: Edward J Britt, MD

Struggling with IBF?

Find out if you qualify for the ISABELA study.

Right now, the ISABELA clinical research study is testing a medication in people with idiopathic pulmonary fibrosis. If you take part in this study, you’ll receive study medication or placebo on top of your standard of care treatment. The study medication is provided at no cost.

Study participants will receive: • Study medication • Study-related medical care • Reimbursement for expenses.

  • Eligibility: 40+ years old; IPF diagnosis in the past 5 years and in stable health
  • Reimbursements:In addition to travel and transport costs, you will be paid up to a total of $600 if you complete this study up to Week 52. For every on-site visit completed after Week 52 you will be paid $50.  Car service; airfare and hotel accommodations for study visits are offered to certain participants.
  • Contact: Call 410-328-1473 or email
  • STUDY STATUS: Enrollment starting soon


Principal Investigators: Edward J Britt, MD

The purpose of the study is to evaluate the effectiveness of an investigational drug. If you have been diagnosed with IPF, then you may qualify to take part in this clinical study.

  • Eligibility: 40 years of age or older, diagnosis with IPF during the past three years
  • Reimbursement: All study-related procedures, medications, and laboratory services at no cost and you will be paid $50 for each completed visit; the study requires 10 visits.
  • Contact: Call 410-328-1473 or email
  • STUDY STATUS: Enrollment starting soon


We are conducting the INSIGHT COPD study because symptoms of chronic obstructive pulmonary disease (COPD) and high body mass index (BMI) overlap. High BMI means that one’s body weight is higher than is ideal for one’s height. There are many medications for patients with COPD, but there is little mention of weight loss as a possible treatment in current research.

We are trying to find out if a lifestyle program that promotes modest weight loss and increased physical activity will improve COPD symptoms for those with a high BMI. We hope that the program will lead to weight loss and better exercise tolerance. We are also looking at the effects on shortness of breath, quality-of-life, and cardiovascular disease risk factors.

  • Principal Investigator: Robert M Reed, MD
  • Eligibility: Patients with COPD that are age 40 or older and are overweight
  • Reimbursements $40 at the baseline visit. $20 at the 12 Month visit. $40 at the 18 Month visit. If you complete all visits and are in the Intervention group, you will receive an additional $50. If you complete all visits and are in the Control Group, you will receive a Fitbit.
  • Contact: Call 410-328-4155 or email
  • STUDY STATUS: Enrolling

Pulmonary Fibrosis Foundation Registry

This study has two overall goals or arms:

The first is to create and maintain a Pulmonary Fibrosis Foundation Patient Registry (hereafter referred to as the National Registry) of patients with interstitial lung disease and/or pulmonary fibrosis. Interstitial lung diseases (ILD) are a group of diseases characterized by progressive fibrosis (scarring) of the lung tissue leading to difficulty breathing.

You are being asked to participate in this study because your physician has determined that you have ILD and/or pulmonary fibrosis. The data which we collect and incorporate into this National Registry will be analyzed with the goals of improving quality of life and improving outcomes of patients with ILD and/or pulmonary fibrosis. This is an observational National Registry which means you will not receive any investigational treatments or investigational drugs. Your disease management and treatment decisions will be determined by you and your health care professional.

The second goal of this study is to create a Pulmonary Fibrosis Foundation Central Biorepository of samples from patients with ILD and/or pulmonary fibrosis. The Central Biorepository will contain biological samples which will be linked to medical information from enrolled patients. We hope to be able to answer questions about ILD and/or pulmonary fibrosis by analyzing these blood samples for specific genes and other markers of disease.

Researchers at institutions across the country will be able to request samples from the Central Biorepository to hopefully assist them in their own research studies into ILD and/or pulmonary fibrosis.