BENITIONSClinical Trial Intelligence

To Compare the PK and Safety of Omalizumab (CT-P39, EU-approved Xolair, and US-licensed Xolair) in Healthy Subjects

Фаза 1 Завершено NCT04018313

ЗаболеваниеHealthy
ФазаФаза 1
СпонсорCelltrion
СтатусЗавершено
Участники176 участн.
ВмешательствоCT-P39, EU-approved Xolair, CT-P39, EU-approved Xolair, US-licensed Xolair
Дата начала28.05.2020
Дата завершения27.03.2021
Публикация результатов11.05.2023

Кратко

A Phase 1, Randomized, Double-blind, Three-arm, Parallel Group, Single-dose Study to Compare the Pharmacokinetics and Safety of Three Formulations of Omalizumab (CT-P39, EU-approved Xolair, and US-licensed Xolair) in Healthy Subjects

Pharmacokinetic Outcome Measures [AUC0-inf] for Part 2

up to day 127 · day*μg/mL

CT-P39 (Part 2)910.9 ± 278.57 day*μg/mL
EU-approved Xolair (Part 2)897.7 ± 270.25 day*μg/mL
US-licensed Xolair (Part 2)926.3 ± 273.30 day*μg/mL
Ratio of geometric least square means105.62 (95% CI 95.91–116.31)

Pharmacokinetic Outcome Measures [AUC0-last] for Part 2

up to day 127 · day*μg/mL

CT-P39 (Part 2)846 ± 251.87 day*μg/mL
EU-approved Xolair (Part 2)843.8 ± 248.04 day*μg/mL
US-licensed Xolair (Part 2)850.0 ± 213.13 day*μg/mL
Ratio of geometric least square means104.00 (95% CI 94.96–113.89)

Pharmacokinetic Outcome Measures [Cmax] for Part 2

up to day 127 · μg/mL

CT-P39 (Part 2)20.08 ± 5.9940 μg/mL
EU-approved Xolair (Part 2)18.24 ± 4.9981 μg/mL
US-licensed Xolair (Part 2)19.43 ± 5.4159 μg/mL
Ratio of geometric least square means113.14 (95% CI 103.15–124.11)

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