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OpenTrials
Completed

NCT Number: NCT00727285

Cystic Fibrosis (CF) Leukocyte Genes as Biomarkers for Novel Therapies

Presently, effectiveness of treatments for CF lung disease is judged by improvement in lung function (FEV1). However, in CF patients, FEV1 can range from severely decreased to normal, and improvements may occur slowly. Thus, clinical trials require many patients over prolonged periods to evaluate medications. As the pace of drug development accelerates, it is no longer possible to test all of the promising candidate therapies using conventional study designs. A sensitive technique for assessing lung inflammation has been developed which uses the expression of genes located in circulating blood cells. Mononuclear cells pass repeatedly through the blood vessels of the lung, and are exposed to many of the inflammatory products that are present in the airways. Over the past 4 years the investigators have identified a small group of candidate genes that are unregulated or downregulated in response to antibiotic treatment. The investigators now propose to prospectively test this method of quantifying lung inflammation in a large group of CF patients undergoing treatment of pulmonary exacerbations. Blood will be sampled before and after antibiotic treatment for a pulmonary exacerbation, and the relative change in gene expression will be compared to improvement in FEV1 and other clinical responses, to determine the utility of this method for use in studies. If successful, this technique could allow for a rapid and noninvasive method to gauge immediate effects by new treatments, and assist caregivers in determining optimal treatment strategies for the individual.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Documented diagnosis of CF.
  • Age 18 years old or greater.
  • Presentation at the start of treatment for a pulmonary exacerbation of CF.
  • Ability to perform reproducible Pulmonary Function Tests.
  • Willingness to comply with study procedure and willingness to provide written consent.

Exclusion criteria

  • Participation in an investigational drug study within one month of enrollment.
  • Presence of a condition or abnormality that, in the opinion of the Principal Investigator (PI), would compromise the safety of the patient or the quality of the data.

Treatment and study plan

Primary outcomes

  1. The Primary analysis is the change in expression of individual and combinations of mononuclear cell genes, obtained pre- and post-antibiotic therapy.

    Time frame: 14-21 days

Secondary outcomes

  1. Correlation of changes in PBMC gene expression with changes in FEV1

    Time frame: 14-21 days

  2. Correlation of changes in PBMC gene expression with changes in WBC counts.

    Time frame: 14-21 days

Sponsors and collaborators

Lead sponsor

National Jewish Health

Other

Collaborators

  • Cystic Fibrosis Foundation

Registry information

Official study title

CF Leukocyte Genes as Biomarkers for Novel Therapies

Important dates

Study start
2008
Primary completion
2011
Study completion
2012
First posted
Aug 1, 2008
Registry last updated
Mar 29, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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