Biomarker Discovery for Novel Drug Development in Idiopathic Pulmonary Fibrosis



Status:Active, not recruiting
Conditions:Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:35 - 80
Updated:5/6/2018
Start Date:October 2012
End Date:June 2018

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Prospective, Longitudinal Cohort Trial of Patients With Idiopathic Pulmonary Fibrosis (IPF) and Healthy Control Patients. Clinical Data, Blood, and Bronchiolavage (BAL) Fluid Will be Collected Over 12 Months.

Drug discovery can take many years especially since most studies to measure effectiveness
depend on clinical outcomes like pulmonary function tests and hospitalizations.

This is an observational study designed to collect information, blood, and bronchoalveolar
lavage fluid in people who have IPF and those who do not. The people who have IPF will be
followed for 12 months to collect more biological samples and record clinically relevant
information.

The goal of this study is to identify new molecular markers that are measurable and reliable
in people who have IPF. It is hoped that these markers can be used in future drug studies to
significantly speed up the process of finding drugs that help.


Inclusion Criteria:

- age 35 to 80 years

- a diagnosis of IPF by consensus criteria

Exclusion Criteria:

- any condition that makes the patient at unacceptable risk for bronchoscopy

- the presence of significant co-existing emphysema on HRCT

- active cigarette smoking (defined as smoking within the last 6 months)

- the presence of a significant co-morbidity felt to limit life expectancy to less than
12 months.

- active listing for lung transplantation

- inability to provide informed consent
We found this trial at
1
site
San Francisco, California 94143
Principal Investigator: Harold Collard, MD
Phone: 415-502-1958
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mi
from
San Francisco, CA
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