CSL787
BiologicalHuman plasma-derived polyvalent immunoglobulin G (IgG) administered via inhalation of an aerosol produced using a nebulizer
NCT Number: NCT04643587
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.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
IKF Pneumologie Institute, Frankfurt, Germany
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
For Part A (SAD) Only:
For Part B (MAD) Only:
Exclusion criteria
Human plasma-derived polyvalent immunoglobulin G (IgG) administered via inhalation of an aerosol produced using a nebulizer
Normal saline (0.9% NaCl)
Time frame: Up to 8 days (healthy volunteers); Up to 21 days (NCFB patients)
Time frame: Up to 8 days (healthy volunteers); Up to 21 days (NCFB patients)
Time frame: Up to 8 days from inhalation
Time frame: Up to 8 days from inhalation
Time frame: Up to 8 days from inhalation
Time frame: Up to 8 days from inhalation
Time frame: Up to 8 days from inhalation
Time frame: Up to 8 days from inhalation
Time frame: Up to 8 days from inhalation
Time frame: Up to 8 days from inhalation
Time frame: On Day 1, after dosing
Time frame: On Day 1, after dosing
Time frame: On Day 1, after dosing
Time frame: On Day 1, after dosing
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
Time frame: On Day 14, after last dose
CSL Behring
Industry
A Phase 1, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Single and Multiple Ascending Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Exploratory Efficacy of Nebulized CSL787 in Healthy Subjects and Subjects With Non-Cystic Fibrosis Bronchiectasis (NCFB)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.