KB001
BiologicalSingle-dose, 3mg/kg or 10mg/kg dose administered intravenously
Other names: KB001-recombinant human anti-Pa PcrV Fab antibody
NCT Number: NCT00638365
The primary objective of this study is to evaluate the safety and tolerability of a single dose of KB001 in Cystic Fibrosis patients infected with Pseudomonas aeruginosa (Pa)
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Notify Me12 year and older
All sexes
Interventional
Phase 1 / Phase 2
University of Alabama, Birmingham, Alabama, United States
CF patients often have lung infections. Pseudomonas aeruginosa (Pa) is the most significant bacteria in CF, with up to 80% of CF patients eventually becoming infected. These patients are often treated with antibiotics with variable results. This study will examine the impact of a single-dose of an investigational drug, KB001, on Pa bacteria in the CF lung.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Positive sweat chloride greater than 60mEq/liter, and/or a genotype with 2 identifiable mutations consistent with CF, and one or more clinical features consistent with the CF phenotype
Exclusion criteria
Single-dose, 3mg/kg or 10mg/kg dose administered intravenously
Other names: KB001-recombinant human anti-Pa PcrV Fab antibody
Placebo single-dose administered intravenously
Time frame: Day 28
Safety assessments were conducted after completion of day 28. AEs were followed through completion of day 56.
Humanigen, Inc.
Industry
A Phase I/II Randomized, Double-Blind, Placebo-Controlled, Single-Dose, Dose Escalation Study of KB001 in Cystic Fibrosis Patients Infected With Pseudomonas Aeruginosa
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.
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