Search Clinical Trials
Our researchers are currently in need of adult and pediatric study participants to help us pursue better treatments and cures. Participants may receive medical evaluations and procedures, study medication, disease-related education and possible financial compensation for time, travel and participation.
Select a Condition or Specialty
- Allergy
- Alpha-1 Antitrypsin Deficiency
- Asthma
- Cardiology
- Chronic Obstructive Pulmonary Disease (COPD)
- COVID-19 (Coronavirus)
- Cystic Fibrosis
- Eczema (Atopic Dermatitis)
- Environmental & Occupational Health
- Eosinophilic Granulomatosis with Polyangiitis (EGPA)
- Food Allergy
- Gastroenterology
- Idiopathic Pulmonary Fibrosis (IPF)
- Interstitial Lung Disease (Pulmonary Fibrosis)
- Lung Cancer
- Nontuberculous Mycobacteria (NTM)
- Oncology
- Pulmonary Hypertension (PH)
- Respiratory (Pulmonary)
- Rheumatology
- Sarcoidosis
- Sleep
All Clinical Trials

ASPIRE: Potentially Slowing Lung Fibrosis in IPF
Researchers are examining whether an investigational medication called buloxibutid can slow down lung scarring and improve breathing for people with idiopathic pulmonary fibrosis (IPF). Volunteers are needed. Learn if you are eligible for the ASPIRE IPF trial
- Gender
- Any
- Ages
- 40+
- Compensation
- Provided
- Time Required
- 8 clinic visits and 8 phone or video calls over approximately 62 weeks.

Idiopathic Pulmonary Fibrosis (IPF) & GERD
The purpose of this study is to measure and accurately identify the presence and severity of gastroesphageal reflux disease (GERD), commonly called acid reflux, in idiopathic pulmonary fibrosis (IPF) patients using the Supraglottic Index (SGI).
- Gender
- Any
- Ages
- 40-95
- Compensation
- Provided
- Time Required
- 5 visits over a 6-month period, visits are every 3 months

Pulmonary Fibrosis & Genetic Factors
The purpose of this study is to investigate inherited genetic factors that play a role in the development of familial pulmonary fibrosis and to identify a group of genes that predispose individuals to develop pulmonary fibrosis.
- Gender
- Any
- Ages
- Not Specified
- Compensation
- Not Provided
- Time Required
- Not Specified

FIBRONEER-SARD: Treating ILD associated with Autoimmune Disease
: With some autoimmune conditions, interstitial lung disease (ILD) can be a complication that worsens breathing and makes it harder for people to live normally. Researchers are investigating a new medication that may be able to help slow lung fibrosis in autoimmune-related ILD cases. Volunteers are needed
- Gender
- Any
- Ages
- 18+
- Compensation
- Provided
- Time Required
- 8 clinic visits over approximately 7 and ½ months
Adult Trials

ASPIRE: Potentially Slowing Lung Fibrosis in IPF
Researchers are examining whether an investigational medication called buloxibutid can slow down lung scarring and improve breathing for people with idiopathic pulmonary fibrosis (IPF). Volunteers are needed. Learn if you are eligible for the ASPIRE IPF trial
- Gender
- Any
- Ages
- 40+
- Compensation
- Provided
- Time Required
- 8 clinic visits and 8 phone or video calls over approximately 62 weeks.

Idiopathic Pulmonary Fibrosis (IPF) & GERD
The purpose of this study is to measure and accurately identify the presence and severity of gastroesphageal reflux disease (GERD), commonly called acid reflux, in idiopathic pulmonary fibrosis (IPF) patients using the Supraglottic Index (SGI).
- Gender
- Any
- Ages
- 40-95
- Compensation
- Provided
- Time Required
- 5 visits over a 6-month period, visits are every 3 months

Pulmonary Fibrosis & Genetic Factors
The purpose of this study is to investigate inherited genetic factors that play a role in the development of familial pulmonary fibrosis and to identify a group of genes that predispose individuals to develop pulmonary fibrosis.
- Gender
- Any
- Ages
- Not Specified
- Compensation
- Not Provided
- Time Required
- Not Specified

FIBRONEER-SARD: Treating ILD associated with Autoimmune Disease
: With some autoimmune conditions, interstitial lung disease (ILD) can be a complication that worsens breathing and makes it harder for people to live normally. Researchers are investigating a new medication that may be able to help slow lung fibrosis in autoimmune-related ILD cases. Volunteers are needed
- Gender
- Any
- Ages
- 18+
- Compensation
- Provided
- Time Required
- 8 clinic visits over approximately 7 and ½ months
Pediatric Trials
Healthy Participant Trials

FIBRONEER-SARD: Treating ILD associated with Autoimmune Disease
: With some autoimmune conditions, interstitial lung disease (ILD) can be a complication that worsens breathing and makes it harder for people to live normally. Researchers are investigating a new medication that may be able to help slow lung fibrosis in autoimmune-related ILD cases. Volunteers are needed
- Gender
- Any
- Ages
- 18+
- Compensation
- Provided
- Time Required
- 8 clinic visits over approximately 7 and ½ months