comparemela.com

Latest Breaking News On - ஹால் பரோன் - Page 26 : comparemela.com

Vir, GSK s experimental COVID-19 treatment moves into a Phase 3 clinical trial

-3.32% gained 1.3% in premarket trading on Friday, the day after the biotech and GlaxoSmithKline GSK, +0.36% said they started dosing patients in a late-stage clinical trial for an experimental antibody-based COVID-19 treatment. The Phase 3 study is part of the National Institutes of Health s Accelerating COVID-19 Therapeutic Interventions and Vaccines Program. The companies are testing VIR-7831 in patients who have been hospitalized due to COVID-19 infections. The investigational treatment has the potential to neutralize the virus and kill infected cells, [which] could allow this treatment to be effective for patients in hospital settings, where other antibodies have so far not shown an impact, GSK chief scientific officer Dr. Hal Barron said in a statement. While at least two coronavirus vaccines have showed an efficacy rate of about 95% in clinical trials, making them highly effective at preventing symptomatic forms of the disease, efforts to develop t

GlaxoSmithKline And Vir Biotechnology Kick Off ACTIV-3 Covid Trial

GlaxoSmithKline And Vir Biotechnology Kick Off ACTIV-3 Covid Trial Thu, 17th Dec 2020 21:45 (Alliance News) - GlaxoSmithKline PLC and Vir Biotechnology Inc said Thursday they have started the US National Institutes of Health sponsored ACTIV-3 trial for evaluating VIR-7831 in hospitalised adults with Covid-19. The pair said that the first patient has been dosed in a new sub-trial of the NIH s Accelerating Covid-19 Therapeutic Interventions & Vaccines Program Phase 3 clinical trial. This trial is designed to evaluate the safety and efficacy of VIR-7831 for the treatment of hospitalised adults with COVID-19. VIR-7831, also known as GSK4182136, is a fully human anti-SARS-CoV-2 investigational monoclonal antibody to treat the virus.

GSK gets FDA nod for Benlysta to treat active lupus nephritis

GSK gets FDA nod for Benlysta to treat active lupus nephritis
pharmaceutical-business-review.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmaceutical-business-review.com Daily Mail and Mail on Sunday newspapers.

FDA approves GSK s BENLYSTA as the first medicine for adult patients with active lupus nephritis in the US

FDA approves GSK s BENLYSTA as the first medicine for adult patients with active lupus nephritis in the US Approval builds on nearly 10 years of experience in lupus News provided by Share this article Share this article LONDON, Dec. 17, 2020 /PRNewswire/  GlaxoSmithKline plc (LSE/NYSE: GSK) announced the US Food and Drug Administration (FDA) has approved BENLYSTA (belimumab) for the treatment of adult patients with active lupus nephritis (LN) who are receiving standard therapy. Lupus nephritis is a serious inflammation of the kidneys caused by systemic lupus erythematosus (SLE), the most common form of lupus, which can lead to end-stage kidney disease, requiring dialysis or a kidney transplant. The approval extends the current indication in the US to include both SLE and LN for both the intravenous and subcutaneous formulations.

© 2024 Vimarsana

vimarsana © 2020. All Rights Reserved.