Overview Safety, Tolerability and Pharmacokinetics of BIIL 284 BS in Adult and Pediatric Cystic Fibrosis (CF) Patients Status: Completed Trial end date: 1969-12-31 Target enrollment: Participant gender: Summary Safety, tolerability and pharmacokinetics following repeated doses (15-day dosing) Phase: Phase 1 Details Lead Sponsor: Boehringer Ingelheim