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Safety and serum distribution of anti-SARS-CoV-2 monoclonal antibody MAD0004J08 after intramuscular injection.

Authors :
Lanini, Simone
Milleri, Stefano
Andreano, Emanuele
Nosari, Sarah
Paciello, Ida
Piccini, Giulia
Gentili, Alessandra
Phogat, Adhuna
Hyseni, Inesa
Leonardi, Margherita
Torelli, Alessandro
Montomoli, Emanuele
Paolini, Andrea
Frosini, Andrea
Antinori, Andrea
Nicastri, Emanuele
Girardi, Enrico
Plazzi, Maria Maddalena
Ippolito, Giuseppe
Vaia, Francesco
Source :
Nature Communications; 4/27/2022, Vol. 13 Issue 1, p1-8, 8p
Publication Year :
2022

Abstract

The emerging threat represented by SARS-CoV-2 variants, demands the development of therapies for better clinical management of COVID-19. MAD0004J08 is a potent Fc-engineered monoclonal antibody (mAb) able to neutralize in vitro all current SARS-CoV-2 variants of concern (VoCs) including the omicron variant even if with significantly reduced potency. Here we evaluated data obtained from the first 30 days of a phase 1 clinical study (EudraCT N.: 2020-005469-15 and ClinicalTrials.gov Identifier: NCT04932850). The primary endpoint evaluated the percentage of severe adverse events. Secondary endpoints evaluated pharmacokinetic and serum neutralization titers. A single dose administration of MAD0004J08 via intramuscular (i.m.) route is safe and well tolerated, resulting in rapid serum distribution and sera neutralizing titers higher than COVID-19 convalescent and vaccinated subjects. A single dose administration of MAD0004J08 is also sufficient to effectively neutralize major SARS-CoV-2 variants of concern (alpha, beta, gamma and delta). MAD0004J08 can be a major advancement in the prophylaxis and clinical management of COVID-19. Monoclonal antibodies (mAbs) are a potential therapeutic option for treatment of COVID-19. Here, the authors report safety and pharmacokinetics of an intramuscularly injected mAb (MAD0004J08) during the first 30 days of a phase 1 clinical study. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
13
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
156548137
Full Text :
https://doi.org/10.1038/s41467-022-29909-x