Journal
JOURNAL OF PHARMACEUTICAL INNOVATION
Volume -, Issue -, Pages -Publisher
SPRINGER
DOI: 10.1007/s12247-023-09713-w
Keywords
COVID-19; SARS-CoV-2; Antibody therapeutics; Neutralizing antibody; Technology foresight
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After almost 3 years of the COVID-19 pandemic, the development and dissemination of knowledge and products have not stopped due to the evolving virus and new variants. This study aims to analyze the current landscape of neutralizing monoclonal antibodies (nAbs) for COVID-19, providing valuable information for decision-making in scientific and pharmaceutical organizations.
PurposeAfter nearly 3 years of the COVID-19 pandemic, even though a vast body of knowledge and products (including vaccines and treatments) have been developed and disseminated, the virus is still evolving and new variants arising. Consequently, thousands of lives continue to be lost. Neutralizing monoclonal antibodies (nAbs) are promising drugs that emerged to treat SARS-CoV-2. In the uncertainty of the current situation, there is the question of whether organizations should continue to invest in this technology. To help decision-making in scientifical and pharmaceutical organizations, it is of major importance to monitor the development of products and technologies. Therefore, the aim of this study is analyze the landscape of nAbs for COVID-19.MethodsThe scenario of 473 biotherapeutics focusing on nAbs was evaluated using foresight techniques and a review of literature. Data were obtained from structured and semi-structured databases and processed for treatment, cleaning, consistency, validation, and enrichment.ResultsWe identified 227 nAbs and performed an extensive literature review of 16 nAbs in late clinical development, including development technologies, responses to variants of concern (VOCs), manufacturing, and clinical aspects.ConclusionsEven though the emergence of new VOCs is a threat to the effectiveness of this treatment, demanding constant genomic surveillance, the use of nAbs to treat and prevent COVID-19 will probably continue to be relevant due to excellent safety profiles and the possibility of immediate immunity transfer, especially in patients showing inadequate immunological response to vaccination. Therefore, we suggest that organizations should keep investing in improvements in this technology.
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