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OpenTrials
Completed

NCT Number: NCT01691612

Role of the Isomerase Pin-1 in the Development and Treatment of Asthma

Pin1 is activated in asthmatic airways, increasing cytokine mRNA stability and eosinophil survival. This study is designed to test whether the Pin1 enzyme regulates TLR/IL-1R signal pathways in multiple cells in asthma.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Asthma Research Center

Boston, Massachusetts, 02115, United States

About this study

The investigators will test their hypothesis that Pin1 regulates TLR/IL-1R signaling pathways in asthma by examining Pin1 and related pathway activation in BAL-derived eosinophils after house dust mite allergen challenge. The investigators will perform segmental allergen challenge. BAL and lung biopsy of the allergen-challenged segments will be performed 48 hr later and activation of Pin1 and related pathways will be examined.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subjects 18-55 years of age, diagnosed with asthma for at least 1 year;
  • And FEV1 > 70% predicted on only short acting beta agonists e.g albuterol
  • And methacholine PC20 < 8 mg/ml
  • Positive skin prick test to Dermatophagoides pteronyssinus(DerP)
  • No prior history of intubation for asthma
  • No use of inhaled corticosteroids for 1 month prior to entry

Exclusion criteria

  • Current smoking or smoking history of greater than 10 pack-years
  • Any other clinically important comorbidity determined by the principal investigator to affect subject safety, including uncontrolled diabetes, uncontrolled coronary artery disease, acute or chronic renal failure, and uncontrolled hypertension that would increase the risk of significant adverse events during bronchoscopy,
  • Worsening of asthma symptoms requiring treatment with steroids within 4 weeks of screening
  • Respiratory infection within four weeks
  • Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant or who are currently pregnant or lactating.

Unless they:

  • Are women whose career, lifestyle, or sexual orientation precludes intercourse with a male partner
  • Are women whose partners have been sterilized by vasectomy or other means
  • Use one acceptable birth control method. Adequate barrier methods of contraception include: diaphragm, condom (by the partner), intrauterine device (copper or hormonal), sponge or spermicide. Hormonal contraceptives include any marketed contraceptive agent that includes an estrogen and/or a progestational agent.
  • Pre-existing lung disease other than asthma
  • History of coagulation disorders or abnormal PT/PTT testing at screening
  • History of immunodeficiency diseases, including HIV
  • A disability that may prevent the patient from completing all study requirements
  • Use of other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer
  • History of malignancy of any organ system (other than localized basal cell carcinoma of the skin), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases.
  • Diagnosis of Hepatitis B or C.
  • History of alcohol abuse (as determined by the principal investigator) within 6 months of screening.
  • History of illicit drug abuse (as determined by the principal investigator) within 6 months of screening.

Treatment and study plan

installation of D. pteronyssinus allergens

Biological

We will perform bronchoscopy and segmental allergen challenges. Subjects will undergo bronchoscopy with segmental installation of 5 ml of D. pteronyssinus (DerP). BAL and lung biopsy of the allergen-challenged segments will be performed 48 hr later

Other names: D. pteronyssinus allergens exposure

Primary outcomes

  1. Change From Baseline in the Percentage of Total White Blood Cell That Were Eosinophils at 48 Hours

    Time frame: from baseline to 48 hours

    Measure Pin1 activity in BAL-derived eosinophils after House Dust Mite (HDM) allergen challenge:

    Eosinophils post-challenge change from pre-challenge is reported: absolute change = [eosinophils post (%) - eosinophils pre (%)]

Secondary outcomes

  1. Percent Change From Baseline in the Percentage of Total White Blood Cell That Were Lymphocytes at 48 Hours

    Time frame: from baseline to 48 hours

    Percent change in percentage of total white blood cell that were lymphocytes is measured from pre-challenge to post-challenge as: [100% * ((Post-Pre)/Pre)]

  2. Percent Change From Baseline in the Percentage of Total White Blood Cell That Were Macrophages at 48 Hours

    Time frame: from baseline to 48 hours

    Percent change in percentage of total white blood cell that were macrophages is measured from pre-challenge to post-challenge as: [100% * ((Post-Pre)/Pre)]

  3. Change From Baseline in the Percentage of Total White Blood Cell That Were Neutrophils at 48 Hours

    Time frame: from baseline to 48 hours

    Neutrophils have some zero values pre-challenge, so absolute change is reported instead of percent change: post-pre from baseline to 48 hours

Sponsors and collaborators

Lead sponsor

Brigham and Women's Hospital

Other

Registry information

Acronym: Pin1

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Sep 25, 2012
Registry last updated
Jul 3, 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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