Cystic Fibrosis Clinical Trial
OBJECTIVES: I. Assess the safety and efficacy of gene transfer into the nasal epithelium
using Ad5-CB-CFTR, an E1-deleted adenovirus vector containing the cystic fibrosis
transmembrane conductance regulator gene, in patients with cystic fibrosis (CF).
II. Determine whether ion transport abnormalities in CF airway cells can be corrected.
PROTOCOL OUTLINE:
Groups of 3 patients receive 1 of 4 doses of Ad5-CB-CFTR, a recombinant E1-deleted
adenovirus serotype 5 vector containing the cystic fibrosis transmembrane conductance
regulator gene. Ad5-CB-CFTR is administered to 1 nasal cavity and the vehicle alone is
administered to the opposite nasal cavity as the control.
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Endpoint Classification: Safety/Efficacy Study, Primary Purpose: Treatment
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