drugset / Trial / NCT00034515

A Study in Adult and Pediatric Patients With Cystic Fibrosis

NCT00034515 ↗

Phase 1/2 Completed 63 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this ascending dose group study is to assess the safety, tolerability, and effects of multiple dose levels of INS37217 and placebo followed by five days twice daily treatment with maximum tolerated dose administered by inhalation via the Pari LC Star nebulizer in adult and pediatric patients with cystic fibrosis

Timeline

Start
2001-06
Primary completion
2002-08
Completion
2002-08

Drugs

EvaluationDrugModalityDoseRoute
Subject denufosol Other / unclassified 10 mg Other
Subject denufosol Other / unclassified 20 mg Other
Subject denufosol Other / unclassified 40 mg Other
Subject denufosol Other / unclassified 60 mg Other

Indications