COVID-19

AstraZeneca Reports Results from the P-III (SUPERNOVA) Study of Sipavibart to Prevent COVID-19 in Immunocompromised Patients

AstraZeneca Reports Results from the P-III (SUPERNOVA) Study of Sipavibart to Prevent COVID-19 in Immunocompromised Patients

Shots: The P-III (SUPERNOVA) study investigates the safety & efficacy of sipav...

Sanofi Partners with Novavax to Co-commercialize COVID-19 Vaccine and Develop Flu-COVID-19 Combination Vaccines

Sanofi Partners with Novavax to Co-commercialize COVID-19 Vaccine and Develop Flu-COVID-19 Combination Vaccines

Shots: Agreement grants co-exclusive rights to Sanofi to co-commercialize Novavax&...

Shionogi Reports the P-III Trial Results for Ensitrelvir as a Treatment of Common COVID-19 Symptoms

Shionogi Reports the P-III Trial Results for Ensitrelvir as a Treatment of Common COVID-19 Symptoms

Shots: The P-II/III (SCORPIO-SR) trial evaluates Ensitrelvir (125/250mg) vs PBO in...

Junshi Biosciences Reports the Result of VV116 in P-III to Treat COVID-19

Junshi Biosciences Reports the Result of VV116 in P-III to Treat COVID-19

Shots: The 2nd P-III study evaluating safety & efficacy of VV116 (mindeudesivi...

Senhwa Bioscience’s Silmitasertib Received the US FDA IND Approval to treat patients with community-acquired pneumonia (CAP)

Senhwa Bioscience’s Silmitasertib Received the US FDA IND Approval to treat patients with community-acquired pneumonia (CAP)

Shots: The US FDA approved P-II IND evaluating silmitasertib (CX-4945) that aimed...

Moderna's Patent Revoked by the European Patent Office (EPO) due to BioNTech Vaccine Dispute

Moderna's Patent Revoked by the European Patent Office (EPO) due to BioNTech Vaccine Dispute

Shots: The European Patent Office declared that Moderna's mRNA patent was inva...

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