Comparing the Efficacy of Symbicort® pMDI and Formoterol Turbuhaler in Reducing Exacerbations in Patients With Cronic Obstructive Pulmonary Disease

A Phase IIIB, 6-Month, Double-blind, Double-dummy, Randomized, Parallel-group, Multicenter
Exacerbation Study of Symbicort® pMDI 160/4.5 μg x 2 Actuations Twice-daily Compared to
Formoterol Turbuhaler 4.5 μg x 2 Inhalations Twice-daily in COPD Patients.

Inclusion Criteria:

3. A current clinical diagnosis of COPD with COPD symptoms for more than 1 year, according
to the GOLD guidelines.

4. Current or previous smoker with a smoking history equivalent to 10 or more pack years (1
pack year = 20 cigarettes smoked per day for 1 year).

5. Post-bronchodilator FEV1/forced vital capacity (FVC) <0.7 (70%) and FEV1 ≤70% of
predicted normal (PN) value.

6. Documented use of a short-acting inhaled bronchodilator (β2-agonists or
anticholinergics) as rescue medication within 6 months prior to study start.

7. A score of ≥2 on the modified medical research council (MMRC) dyspnea scale. 8.
Documented history of ≥1 moderate or severe COPD exacerbation(s) that required treatment
with systemic (oral, IM, IV) corticosteroids (a minimum 3 day course of an oral
corticosteroid treatment or single depot corticosteroid injection), or hospitalization
(defined as an inpatient stay or >24 hour stay in an observation area in the emergency
department or other equivalent facility depending on the country and healthcare system)
within 2-52 weeks before Visit 1 (i.e., not within the 14 days prior to Visit 1). A history
of an exacerbation treated exclusively with antibiotics will not be considered adequate.

Exclusion Criteria:

1. A history of asthma at or after 18 years of age.

2. Subjects with significant or unstable ischemic heart disease, arrhythmia,
cardiomyopathy, heart failure (including significant cor pulmonale), uncontrolled
hypertension as defined by the Investigator, or any other relevant cardiovascular
disorder as judged by the Investigator.

3. Known homozygous alpha-1 antitrypsin deficiency.

4. Any significant disease or disorder (e.g., gastrointestinal, liver, renal,
neurological, musculoskeletal, endocrine, metabolic, malignant, psychiatric, major
physical impairment) which, in the opinion of the Investigator, may either put the
subject at risk because of participation in the study, or influence the results of the
study, or the subject's ability to participate in the study.

5. A history of malignancy (except basal cell carcinoma) within the past 5 years.

6. Active tuberculosis, lung cancer, bronchiectasis, sarcoidosis, lung fibrosis, primary
pulmonary hypertension, interstitial lung disease, or other active pulmonary diseases.

7. Subjects who have needed additions or alterations to their usual maintenance or change
in formulation of rescue therapy for COPD due to worsening symptoms within the 14 days
prior to Visit 1 and up to Visit 3.

8. CXR (frontal and lateral) with suspicion of pneumonia or other condition/abnormality
that will require additional investigation/treatment, or put the subject at risk
because of participation in the study.

9. Risk factors for pneumonia: immune suppression (HIV, lupus) or other risk for
pneumonia (e.g. neurological disorders affecting control of the upper airway, such as
Parkinson's disease, myasthenia gravis, etc.).

10. Pneumonia not resolved within 14 days of Visit 1.

11. Moderate or severe COPD exacerbation that has not resolved within 14 days prior to
Visit 1 or a moderate or severe COPD exacerbation that occurs between Visit 1 and
Visit 2.

12. Long-term oxygen therapy (LTOT) or nocturnal oxygen therapy required for greater than
12 hours a day.

13. Subjects who are currently in the intensive rehabilitation phase or scheduled to begin
new participation (intensive rehabilitation phase) in a pulmonary rehabilitation
program during the study or have started a new pulmonary rehabilitation program within
60 days of Visit 1. Subjects in the maintenance phase of pulmonary rehabilitation
program are not excluded.

14. Treatment with oral, parenteral, or intra-articular corticosteroids within 4 weeks
prior to Visit 1.

15. Omalizumab or any other monoclonal or polyclonal antibody therapy taken for any reason
within 6 months prior to Visit 1.