This study will look at the pharmacokinetics, safety, toleration and efficacy of PF-00610355 in the chronic obstructive pulmonary disease (COPD) population. The doses in this study are intended to explore the anticipated clinical dose range.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
20
dry powder inhaler, 1472 mcg, single dose
dry powder inhaler, 736 mcg, single dose
dry powder inhaler, 368 mcg, single dose
Pfizer Investigational Site
Berlin, Germany
Pfizer Investigational Site
Wiesbaden, Germany
To characterize the single dose pharmacokinetics of inhaled PF-00610355 in COPD patients.
Time frame: up to 8 days post dose
To evaluate the safety & toleration of single inhaled doses of PF-00610355 in COPD patients
Time frame: up to 24 hours post dose
To investigate the efficacy of a single inhaled dose of PF-00610355 in COPD patients.
Time frame: up to 24 hours post dose
To investigate the exposure/response relationship of PF-00610355.
Time frame: up to 8 days post dose
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Placebo