The objective of this study is to assess the safety and effects of administration of human corticotropin-releasing factor (hCRF) by continuous IV infusion at rates up to 5 ug/kg/hr for 24 hours in patients with asthma. Patients who present to the hospital for treatment of an acute exacerbation of asthma, and who have failed to respond after receiving standard therapy for at least one hour will be enrolled to this protocol. The study design is an open-label dose escalation, followed by a double-blind, randomized, placebo-controlled comparison of the highest tolerated dose level of hCRF vs. placebo.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR005096-09S1
Application #
6298293
Study Section
Project Start
1997-12-01
Project End
1999-06-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
9
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Tulane University
Department
Type
DUNS #
City
New Orleans
State
LA
Country
United States
Zip Code
70118
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