drugset / Trial / NCT04643587

Study to Assess CSL787 in Non-cystic Fibrosis Bronchiectasis (NCFB)

NCT04643587

Phase 1 Completed 64 enrolled CSL Behring
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study is a prospective, multicenter, randomized, double-blind, placebo-controlled study to investigate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and exploratory efficacy of nebulized CSL787 after administrations of single (SAD) ascending doses in healthy subjects and multiple (MAD) ascending doses in subjects with NCFB.

Timeline

Start
2020-12-07
Primary completion
2023-03-12
Completion
2023-03-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Immune Globulin Intravenous (Human) Protein / enzyme biologic Inhaled

Indications