Rosiglitazone Versus Theophylline in Asthmatic Smokers

Smoking asthmatics have chronic pulmonary inflammation that is relatively steroid resistant. PPAR agonists (of which rosiglitazone is one example) have been shown to reduce several markers of inflammation in humans and in smoking animal models.

This clinical study will use smoking asthmatics as a human model of smoke-induced steroid-insensitive airway inflammation to evaluate both efficacy of rosiglitazone as an anti-inflammatory drug as well as the effect of low doses of theophylline on the response to low-dose inhaled corticosteroid (LD ICS).

Mild or moderate (as per GINA guidelines) persistent-asthmatic smokers will be randomised into this study after a 4-week washout period during which they will be withdrawn from inhaled corticosteroids (ICS). Subjects will then receive one of four treatments for 28 days: rosiglitazone, LD ICS, theophylline, or LD ICS plus theophylline.

The effects of rosiglitazone and LD ICS on pulmonary function will be compared as a primary objective. In addition, effects of theophylline plus LD ICS will be compared against theophylline and LD ICS separately. Both pulmonary anti-inflammatory and systemic anti-inflammatory activity will also be investigated.

Subjects will have baseline assessments of pulmonary function, biomarkers of systemic inflammation, sputum, exhaled breath biomarkers, asthma control questionnaires and safety parameters. Following 28 days of treatment, these parameters will all be reassessed in all subjects.

Inclusion criteria

• Males or females between 18 and 60 years of age (inclusive).
• Clinical diagnosis of mild or moderate persistent asthma in accordance with the Global Initiative for Asthma (GINA) criteria
• Have had a history of asthma for a minimum of 6 months prior to entry into the study
• Subjects must be current cigarette smokers with a minimum five-pack-year smoking history
• Baseline FEV1 that is greater than 50% predicted; and reversibility of 12% or more at screening, washout or randomisation.
• Capable of providing signed written informed consent and complying with all the specified study procedures.

Exclusion criteria

• Asthma exacerbation or a respiratory tract infection within four weeks of screening.
• Type 1 or type 2 diabetes mellitus.
• Women who are lactating, pregnant, or planning to become pregnant.
• Clinically significant renal or hepatic laboratory values (e.g. AST/ALT/total bilirubin/AP > 2.5 times normal values).
• Anaemia (< 11 g/dL for males or < 10 g/dL for females)
• Contraindications to treatment as outlined in any of the product labels
• Prior history of severe oedema or serious fluid related event (e.g., heart failure) associated with any TZD
• The subject has a history of significant hypersensitivity to study drugs
• Presence of unstable or severe angina or congestive heart failure (NYHA class III/IV) or evidence or history of known congestive heart failure (NYHA class I-IV) or an abnormal electrocardiogram (ECG), as determined by the Investigator, or subjects who have had new cardiac events (such as MI, new CHF, PTCA, CABG) within 6 months of screening.
• History or suspicion of current drug abuse or alcohol abuse within the last 6 months.
• History suggestive of active infection or non-asthma lung pathology
• Clinically significant renal disease, metabolic syndrome, cirrhosis (Child-Pugh Class B/C), hypertension or any other clinically significant cardiovascular, neurological, endocrine, or haematological abnormalities that are uncontrolled on permitted therapy.
• Risk factors for human immunodeficiency virus (HIV), hepatitis B or hepatitis C infection at Screening (Visit 1)
• Subjects who are morbidly obese, defined as having a body mass index (BMI) > 40 kg/m2
• Unable to perform spirometry
• Subjects who require treatment with any of the following asthma medications from Screening (Visit 1) until study completion:

• Inhaled cromolyn sodium or nedocromil;
• Ipratropium bromide;
• Xanthines (theophylline preparations);
• Leukotriene modifiers;
• Long-acting inhaled beta2-agonists (salmeterol, formoterol);
• Oral beta2-agonists.
• Treatment with oral, intravenous or intra-articular corticosteroids within 6 weeks of Screening or thereafter.
• Subjects who have been taking in excess of 1000 μg daily of beclomethasone (or equivalent) within 6 weeks of Screening