EMA fast-tracks review of AstraZeneca's sipavibart to stop Covid [Yahoo! Finance]
AstraZeneca PLC - American Depositary Shares (AZN)
Last astrazeneca plc - american depositary shares earnings: 2/5 04:00 pm
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Source: Yahoo! Finance
prophylaxis (preventive treatment) in immunocompromised patients, under an accelerated assessment approach. A long-acting antibody, sipavibart has been designed to neutralise the spike protein interaction with the ACE2 receptor, providing protection from Omicron and other ancestral viral variants. Licensed from RQ Biotechnology in May 2022, the antibody has been developed to safeguard immunocompromised individuals from Covid-19. These patients are at a heightened risk of severe outcomes from the disease. The EMA's Committee for Medicinal Products for Human Use (CHMP) granted sipavibart an accelerated assessment due to its potential for public health and as a therapeutic innovation. The submission for sipavibart is based on the positive outcomes from the Phase III SUPERNOVA clinical trial. This international, double-blind, randomised, placebo-controlled trial analysed the efficacy and safety of sipavibart versus control (tixagevimab/cilgavimab or placebo). The variants of C
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AZN
Sec Filings
- 7/1/24 - Form 6-K
- 7/1/24 - Form 6-K
- 6/26/24 - Form 11-K
- AZN's page on the SEC website