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Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Azithromycin
Placebo
Sponsored by
NYU Langone Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, pulmonary disease

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers
  • Key Inclusion Criteria: List primary criteria for study inclusion (i.e. do not need to enter entire list of inclusion criteria).

    1. Patient must be 50 years old or older.
    2. Patient must have a smoking history of at least 20 pack-years
    3. Patient must have stable COPD, GOLD 0, I and/or IIA.
    4. CT of chest with evidence of emphysema
  • Key Exclusion Criteria: List primary criteria for study exclusion (i.e. do not need to enter entire list of inclusion criteria).

    1. FEV1 < 70%.
    2. Exacerbations (defined as use of oral steroids or antibiotics) in the previous month.
    3. Cardiovascular Disease defined as abnormal EKG, known or suspected coronary artery disease or congestive heart failure.
    4. Diabetes mellitus
    5. Renal disease
    6. Liver disease
    7. Lung cancer
    8. ETOH use of more than >6 beers >4 mixed drinks daily

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Azithromycin

    Placebo

    Arm Description

    Azithromycin 250mg daily, single daily use for 8 weeks

    Placebo daily for 8 weeks

    Outcomes

    Primary Outcome Measures

    Inflammatory markers
    Cytokines in BAL in pg/mL

    Secondary Outcome Measures

    transcription factor changes
    BAL cell differential in percentage
    Lung function changes
    Forced Vital Capacity (FVC)

    Full Information

    First Posted
    September 2, 2015
    Last Updated
    March 19, 2019
    Sponsor
    NYU Langone Health
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02557958
    Brief Title
    Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study
    Official Title
    Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2009 (Actual)
    Primary Completion Date
    December 2018 (Actual)
    Study Completion Date
    December 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    NYU Langone Health

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    Yes
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study.
    Detailed Description
    Chronic Obstructive Pulmonary Disease (COPD) is the 4th leading cause of death in the United States. It is projected to be the leading cause of death by 2020. As many as 24 million Americans are estimated to suffer from impaired lung function. Of those more than 12 million were actually diagnosed with COPD, and over 118,000 deaths were attributed to COPD in 2004. COPD has been linked with an increased risk for lung cancer. Both airway obstruction, defined by abnormal pulmonary function tests (PFTs), and CT scan diagnosed emphysema were shown to be independent risk factors for lung cancer. Treatment for COPD includes cessation of environmental exposures (i.e. smoking), dampening the inflammatory response, symptoms control and, for a small subgroup, surgical approaches and lung transplant. Nevertheless, the effectiveness of these treatment options to change the natural history of this disease is very limited. Recent evidence suggests a new role for macrolides as immune-modulators in patients with COPD, although the mechanisms are not clearly determined. The investigators hypothesize that in patients with COPD, treatment with azithromycin will show reduced inflammatory markers, transcription factors changes, and lung function changes consistent with reduced inflammation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Obstructive Pulmonary Disease
    Keywords
    COPD, pulmonary disease

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    19 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Azithromycin
    Arm Type
    Experimental
    Arm Description
    Azithromycin 250mg daily, single daily use for 8 weeks
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo daily for 8 weeks
    Intervention Type
    Drug
    Intervention Name(s)
    Azithromycin
    Other Intervention Name(s)
    Zithromax
    Intervention Description
    We hypothesize that in patients with COPD, treatment with azithromycin will show reduced inflammatory markers, transcription factors changes, and lung function changes consistent with reduced inflammation.
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    We hypothesize that in patients with COPD, treatment with placebo will show NO change in inflammatory markers, transcription factor changes and lung function from baseline.
    Primary Outcome Measure Information:
    Title
    Inflammatory markers
    Description
    Cytokines in BAL in pg/mL
    Time Frame
    outcome will be assessed up to two months post initial bronchoscopy
    Secondary Outcome Measure Information:
    Title
    transcription factor changes
    Description
    BAL cell differential in percentage
    Time Frame
    outcome will be assessed up to two months post initial bronchoscopy
    Title
    Lung function changes
    Description
    Forced Vital Capacity (FVC)
    Time Frame
    outcome will be assessed up to two months post initial bronchoscopy

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Key Inclusion Criteria: List primary criteria for study inclusion (i.e. do not need to enter entire list of inclusion criteria). Patient must be 50 years old or older. Patient must have a smoking history of at least 20 pack-years Patient must have stable COPD, GOLD 0, I and/or IIA. CT of chest with evidence of emphysema Key Exclusion Criteria: List primary criteria for study exclusion (i.e. do not need to enter entire list of inclusion criteria). FEV1 < 70%. Exacerbations (defined as use of oral steroids or antibiotics) in the previous month. Cardiovascular Disease defined as abnormal EKG, known or suspected coronary artery disease or congestive heart failure. Diabetes mellitus Renal disease Liver disease Lung cancer ETOH use of more than >6 beers >4 mixed drinks daily

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    27486204
    Citation
    Segal LN, Clemente JC, Wu BG, Wikoff WR, Gao Z, Li Y, Ko JP, Rom WN, Blaser MJ, Weiden MD. Randomised, double-blind, placebo-controlled trial with azithromycin selects for anti-inflammatory microbial metabolites in the emphysematous lung. Thorax. 2017 Jan;72(1):13-22. doi: 10.1136/thoraxjnl-2016-208599. Epub 2016 Aug 2.
    Results Reference
    derived

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    Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study

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