Stopped: The termination was due to business reasons. No safety or efficacy concerns contributed to the termination of the study
The study proposes to evaluate the safety and efficacy of PF-03715455 in moderate to severe asthma when added to standard of care and during staged withdrawal of background therapy.
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Percentage of Participants With Asthma Worsening Events
Timeframe: Baseline up to follow-up period (Week 16)