A Phase 1 interventional study of IMA-638 in Asthma, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer. Completed at 1 site in United States. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2007-12-05.
Sponsored by Wyeth is now a wholly owned subsidiary of Pfizer · Phase 1, Interventional, and Diagnostic
The purpose of this study is to evaluate the safety of, and blood drug levels for, single, ascending doses of IMA-638 in mild to moderate asthma subjects.
3,921 studies on the registry are indexed under Asthma; 507 are open to participants now.
Browse Asthma studies →Wyeth is now a wholly owned subsidiary of Pfizer is the lead sponsor of 472 studies on the registry; none are open to participants now.
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Inclusion Criteria:
Safety will be measured by evaluating physical examinations, spirometry, vital signs, electrocardiograms (ECGs), and clinical laboratory test results.
Drug levels in the blood and associated biomarkers will be evaluated.
This study is completed, as verified in Dec 2007. You cannot join it, but the record below documents what was studied.
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Wyeth is now a wholly owned subsidiary of Pfizer