A Randomized, Placebo-Controlled, Double-Blind Pilot Study of Pioglitazone Hydrochloride in Severe, Refractory Asthma
| Status: | Completed |
|---|---|
| Conditions: | Asthma, Pulmonary |
| Therapuetic Areas: | Pulmonary / Respiratory Diseases |
| Healthy: | No |
| Age Range: | 18 - 75 |
| Updated: | 2/16/2017 |
| Start Date: | September 23, 2009 |
| End Date: | June 24, 2016 |
Background:
- Individuals who have severe asthma that is not easily controlled by current treatments are
in need of new treatments to prevent potentially life-threatening asthma attacks.
Experiments in mice have found that a medication called pioglitazone hydrochloride (Actos ),
which is used to treat patients with diabetes, may be effective for treating severe asthma.
Researchers are interested in determining whether Actos is effective in improving the
quality of life in subjects with severe asthma who continue to have symptoms despite maximum
standard medical therapy.
Objectives:
- To assess the effectiveness of pioglitazone hydrochloride as a treatment for patients with
severe asthma that is not controlled by standard treatments.
Eligibility:
- Individuals between 18 and 75 years of age who have been diagnosed with and treated for
severe asthma for at least 1 year.
Design:
- Potential participants will have a screening visit to determine eligibility for the
study. The visit will involve breathing tests, chest x rays, heart and lung monitoring,
and blood tests.
- Eligible participants will have a full medical history and will answer a series of
questionnaires about their quality of life with asthma.
- Phase 1: Patients will record lung function and asthma symptoms morning and evening for
4 weeks. At the end of this period, patients will be evaluated with breathing, allergy,
and blood tests, as well as questionnaires. Patients will also provide a sputum sample.
- Phase 2: Patients will receive regular doses of either pioglitazone hydrochloride or a
placebo for 16 weeks. Patients will return to the National Institutes of Health every 4
weeks for tests.
- Phase 3: Wash-out period without study drugs for 4 weeks, similar to Phase 1.
- Phase 4: Patients will receive regular doses of either pioglitazone hydrochloride or a
placebo for 16 weeks. Patients who received placebo will be given the study drug, and
vice versa. Patients will return to the National Institutes of Health every 4 weeks for
tests.
- Phase 5: Medications will be stopped, and patients will return to the National
Institutes of Health 4 weeks later for final tests.
- Individuals who have severe asthma that is not easily controlled by current treatments are
in need of new treatments to prevent potentially life-threatening asthma attacks.
Experiments in mice have found that a medication called pioglitazone hydrochloride (Actos ),
which is used to treat patients with diabetes, may be effective for treating severe asthma.
Researchers are interested in determining whether Actos is effective in improving the
quality of life in subjects with severe asthma who continue to have symptoms despite maximum
standard medical therapy.
Objectives:
- To assess the effectiveness of pioglitazone hydrochloride as a treatment for patients with
severe asthma that is not controlled by standard treatments.
Eligibility:
- Individuals between 18 and 75 years of age who have been diagnosed with and treated for
severe asthma for at least 1 year.
Design:
- Potential participants will have a screening visit to determine eligibility for the
study. The visit will involve breathing tests, chest x rays, heart and lung monitoring,
and blood tests.
- Eligible participants will have a full medical history and will answer a series of
questionnaires about their quality of life with asthma.
- Phase 1: Patients will record lung function and asthma symptoms morning and evening for
4 weeks. At the end of this period, patients will be evaluated with breathing, allergy,
and blood tests, as well as questionnaires. Patients will also provide a sputum sample.
- Phase 2: Patients will receive regular doses of either pioglitazone hydrochloride or a
placebo for 16 weeks. Patients will return to the National Institutes of Health every 4
weeks for tests.
- Phase 3: Wash-out period without study drugs for 4 weeks, similar to Phase 1.
- Phase 4: Patients will receive regular doses of either pioglitazone hydrochloride or a
placebo for 16 weeks. Patients who received placebo will be given the study drug, and
vice versa. Patients will return to the National Institutes of Health every 4 weeks for
tests.
- Phase 5: Medications will be stopped, and patients will return to the National
Institutes of Health 4 weeks later for final tests.
New therapies are needed for patients with asthma who are sub-optimally controlled by
standard measures. Pioglitazone hydrochloride (Actos ) is a highly selective and potent
agonist for the peroxisome proliferator-activated receptor-Gamma (PPAR Gamma). Studies in
murine models of allergic asthma have shown that PPAR Gamma agonists down-regulate
allergen-mediated airway inflammation and airway hyperresponsiveness. This protocol is a
randomized, placebo-controlled, doubleblind, crossover (phase II) pilot study of the
efficacy of pioglitazone for the treatment of patients with severe, refractory asthma. The
primary end-point for this study will be quality of life as determined by the Asthma Quality
of Life Questionnaire (AQLQ) score. Secondary end-points will include indices of airway
inflammation, airflow obstruction, airway hyperreactivity, and asthma symptoms.
standard measures. Pioglitazone hydrochloride (Actos ) is a highly selective and potent
agonist for the peroxisome proliferator-activated receptor-Gamma (PPAR Gamma). Studies in
murine models of allergic asthma have shown that PPAR Gamma agonists down-regulate
allergen-mediated airway inflammation and airway hyperresponsiveness. This protocol is a
randomized, placebo-controlled, doubleblind, crossover (phase II) pilot study of the
efficacy of pioglitazone for the treatment of patients with severe, refractory asthma. The
primary end-point for this study will be quality of life as determined by the Asthma Quality
of Life Questionnaire (AQLQ) score. Secondary end-points will include indices of airway
inflammation, airflow obstruction, airway hyperreactivity, and asthma symptoms.
- INCLUSION CRITERIA:
- Subjects will be between 18 and 75 years of age, male or female, with a diagnosis of
severe, refractory asthma, as defined by the American Thoracic Society, for at least
one year.
- Subjects must have a history of reversible airflow obstruction as defined by a
positive methacholine bronchoprovocation challenge or a positive response to inhaled
bronchodilators at some point in the course of their disease or a greater than 20%
variability in the Forced Expiratory Volume in 1 second (FEV1) or the peak expiratory
flow (PEF) documented during serial measurements of lung function over time.
- Left ventricular ejection fraction greater than or equal to 50% by echocardiogram
- For women of childbearing potential, negative pregnancy test prior to study and
willingness to adhere to reliable birth control methods during the study.
- Subjects must have the ability to provide informed consent
EXCLUSION CRITERIA:
- A known history of hypersensitivity to pioglitazone.
- Asthma exacerbation requiring treatment with additional oral corticosteroids in the
previous 6 weeks, or a life-threatening asthma attack requiring cardiopulmonary
support in the previous 6 months.
- Cigarette smoking within the previous 12 months or a prior history of > 20 cumulative
pack-years.
- Investigational therapy for any indication within I month prior to the screening
visit.
- History of lung disease other than asthma (ie., COPD, sarcoidosis).
- History of diabetes mellitus requiring treatment with any medication, insulin
secreting tumor, or symptomatic hypoglycemia.
- HIV/AIDS
- History of congestive heart failure with current symptoms consistent with NYHA
classification II, Ill or IV.
- Preexisting edema (2+ or greater).
- Hemoglobin < 11 gm/dl for males and < 10 gm/dl for females.
- Active liver disease or abnormal liver function tests > 2 times upper limit of
normal.
- History of bladder or colon cancer.
- History of other cancer not in remission.
- Active breast feeding.
- Use of the following medications, which can interact with pioglitazone:
- Gemfibrizol (Lopid)
- Atazanivir (Reyataz)
- Ritonavir (Norvir)
- Rifampin (Rifadpin)
- Carbamzepine (Tegretol)
- Phenobarbital (Luminal)
- Phenytoin (Dilantin)
- Rifapentine (Priftin)
- Secobarbital (Seconal)
- Amiodarone (Cordarone, Pacerone)
- Palitaxel (Taxol)
- Replaglinide (Prandine)
- Ketoconazole (Nizoral)
- Atorvastatin (Lipitor )
- Fosphenytoin (Cerebyx)
- Itraconazole (Sporanox)
- Trimethoprim (in Bactrim)
- Thioridazine
- Certain over-the-counter herbs and supplements. These will be reviewed by the
investigators for possible interactions with the study medication A determination of
whether the supplement is safe to use with pioglitazone will be made on a
case-by-case basis.
- Any condition that, in the investigator s opinion, places the patient at undue risk
for complications from pioglitazone therapy.
We found this trial at
2
sites
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
Phone: 800-411-1222
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