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March 16, 2022
Press release content from Business Wire. The AP news staff was not involved in its creation.
March 16, 2022
The Independent Data Monitoring Committee recommended that the EMPA-KIDNEY trial be stopped early, following a formal interim assessmentEMPA-KIDNE...
March 5, 2022
The FINANCIAL -- The RECOVERY trial has demonstrated that baricitinib reduces the risk of death when given to hospitalised patients with severe COVID-19. Baricitinib is an anti-inflammatory treatment normally used to treat rheumatoid arthritis. According to UKRI, the benefit was in addition to those of dexamethasone and tocilizumab, two other anti-inflammatory treatments that have previously beenThe FINANCIAL -- The RECOVERY trial has demonstrated that baricitinib reduces the risk of death when ...
March 3, 2022
Rheumatoid arthritis drug baricitinib can reduce risk of death from severe Covid by about a fifth
January 19, 2022
Corticosteroids have been advised as a drug to target the host immune response in patients affected with severe lung inflammation due to COVID-19.
January 1, 2022
Vir Biotechnology Announces New Research Describing the Structural Basis of SARS-CoV-2 Omicron Immune Evasion and Receptor Engagement - read this article along with other careers information, tips and advice on BioSpace
December 8, 2021
Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the European Commission has extended the marketing authorisation for Actemra®/RoActemra® (tocilizumab) to include the treatment of COVID-19 in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation.1 This ...
December 7, 2021
EMA's CHMP recommended the approval yesterdayApproval based on results from four phase III studies in over 5,500 patientsActemra/RoActemra has also been provisionally approved in Australia for the treatment
December 7, 2021
Investegate announcements from F. Hoffmann-La Roche Ltd, Actemra/RoActemra approved by the European Commission to treat patients with severe COVID-19
December 7, 2021
The CHMP recommends EU approval for Roche's (RHHBY) Actemra to treat patients with severe COVID-19.