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Clinical Trial Summary

A double-blind, active-controlled, multiple-ascending dose, safety study of aerosolized RSP-1502 in subjects with cystic fibrosis Pseudomonas aeruginosa lung infection.


Clinical Trial Description

This dose escalation safety study will evaluate several doses of RSP-1502 or active control administered by inhalation for 14 days. Following determination of the MTD, a dose expansion cohort will receive RSP-1502 at the MTD versus active control administered by inhalation for 14 days. All subjects will be followed for 14 days after completion of dosing. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06016088
Study type Interventional
Source Respirion Pharmaceuticals Pty Ltd
Contact Brian Jones, PhD
Phone 215-732-5452
Email bjones@respirionpharma.com
Status Recruiting
Phase Phase 1/Phase 2
Start date April 1, 2024
Completion date April 2025

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