Coronavirus disease (COVID-19) is an infectious disease caused by the coronavirus SARS-CoV-2. Here we have collected APR news related to the COVID-19 pandemic, vaccination efforts and emerging treatments.
InflaRx announced the commercial launch of Gohibic (vilobelimab) in the US In April 2023, Gohibic was granted an Emergency Use Authorization (EUA) by the FDA for the treatment of COVID-19 in ...
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The FDA has approved the oral antiviral Paxlovid (nirmatrelvir tablets and ritonavir tablets, co-packaged for oral use) for the treatment of mild-to-moderate COVID-19 in adults who are at high risk ...
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Wednesday, April 19, 2023
The FDA amended the emergency use authorizations (EUAs) of the Moderna and Pfizer-BioNTech COVID-19 bivalent mRNA vaccines to simplify the vaccination schedule for most individuals.
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As the world races towards a post-pandemic future, the surge in demand for single-use systems (SUS) and devices is revolutionizing the production of biologics and vaccines. In BioPlan’s 19th Annual ...
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Sometimes (well, maybe more than that) I get a little frustrated with society. It’s almost like we have given up on thinking for ourselves; having a little common sense.
One example of this is the ...
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CSL officially opened a new state-of-the-art research and development (R&D) center in Waltham, Massachusetts.
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Throughout the COVID-19 pandemic, to protect the health and safety of Canadians, the Government of Canada has taken a prudent and measured approach to adjusting border measures.
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A Kaiser Permanente study confirms the benefit of nirmatrelvir-ritonavir, also known as Paxlovid, as an early-stage treatment to prevent hospitalization for people with mild to moderate COVID-19, ...
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Tuesday, February 14, 2023
Novavax, Inc. announced a modification to its existing agreement with the U.S. Department of Health and Human Services (HHS), in collaboration with the Department of Defense, to deliver up to 1.5 ...
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Wednesday, February 08, 2023
BD (Becton, Dickinson and Company) has received Emergency Use Authorization from the U.S. Food and Drug Administration (FDA) for a new molecular diagnostic combination test for SARS-CoV-2, Influenza A...
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Wednesday, February 01, 2023
Translocation from cytoplasm to nucleus and integration of reverse-transcribed SARS-CoV-2 spike mRNA into the genomic DNA of COVID-19 mRNA-vaccinated individuals positive for HIV-1 or other retroviral...
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The FDA revised the Emergency Use Authorization (EUA) for Evusheld (tixagevimab co-packaged with cilgavimab) to limit its use to when the combined frequency of non-susceptible SARS-CoV-2 variants ...
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Thursday, December 29, 2022
Hetero, India's leading pharmaceutical company with the widest global reach, today announced the receipt of World Health Organization Prequalification of Medicines Program (WHO PQ) approval for its ...
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Thursday, December 22, 2022
BioNTech SE and Shanghai Fosun Pharmaceutical (Group) Co., Ltd. announced that the companies provided approximately 11,500 doses of mRNA-based COVID-19 vaccines which arrived on the Chinese Mainland ...
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Thursday, December 22, 2022
The FDA has approved a new indication for Actemra (tocilizumab) injection for the treatment of hospitalized adult patients with COVID-19 who are receiving systemic corticosteroids and require ...
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