COPD Clinical Trial
Official title:
A 2-Year, Dose Range-Finding, Adaptive-Design Study of the Effects of SCH 527123 in Subjects With Moderate to Severe COPD
Neutrophils are thought to play an important role in the pathophysiology of chronic
obstructive pulmonary disease (COPD). Navarixin (SCH 527123, MK-7123) is an antagonist of the
cysteine-X-cysteine chemokine receptor 2 (CXCR2) and is thought to reduce neutrophil
migration to the diseased lung. It is theorized that reducing neutrophil migration to the
diseased lung will improve a participant's symptoms and the natural history of the disease.
The study will consist of a 2-week screening period followed by a 2-year (104-week)
double-blind treatment period. The 2-year Treatment Period will be made up of two phases: a
26-week (6-month) dose range-finding phase with 3 active arms and 1 placebo arm (Period 1),
followed by a 78-week (18-month) long-term safety and efficacy phase (Period 2). Participants
participating in the original 6-month study (Period 1) may elect not to continue into the
18-month extension study (Period 2).
Hypothesis: navarixin, 50 mg, or the highest remaining dose if the 50-mg dose is
discontinued, is superior to placebo with respect to improving airflow.
n/a
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