drugset / Trial / NCT00274313

Safety Study of Inhaled 552-02 in Cystic Fibrosis Patients

NCT00274313 ↗

Phase 1/2 Completed 40 enrolled Parion Sciences
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of a new inhaled sodium-channel blocker called 552-02 in teens and adults with cystic fibrosis. 552-02 will be inhaled once a day for 14 days using a nebulizer. A small subgroup of patients will donate blood samples for pharmacokinetic analysis to see how 552-02 is absorbed into the blood and eliminated after 14 days of treatment.

Timeline

Start
2006-01
Primary completion
—
Completion
2006-08

Drugs

EvaluationDrugModalityDoseRoute
Subject GS-9411 Small molecule — Inhaled

Indications