Welcome to our dedicated page for Vir Biotechnology news (Ticker: VIR), a resource for investors and traders seeking the latest updates and insights on Vir Biotechnology stock.
Vir Biotechnology, Inc. reports developments as a clinical-stage biopharmaceutical company developing medicines for serious infectious diseases and cancer. Recurring updates cover its chronic hepatitis delta program, including the investigational combination of tobevibart and elebsiran, and its oncology portfolio of PRO-XTEN® dual-masked T-cell engagers across solid tumor targets.
Company news also includes clinical data presentations, trial progress, financial results, equity financing activity, and strategic collaborations. Its VIR-5500 program is a PSMA-targeted PRO-XTEN® dual-masked T-cell engager for metastatic prostate cancer, and the company also describes preclinical work across infectious diseases and oncologic malignancies.
Eli Lilly, Vir Biotechnology, and GlaxoSmithKline announced promising topline results from the Phase 2 BLAZE-4 trial, showing that the combination of bamlanivimab and VIR-7831 significantly reduced high viral loads in low-risk COVID-19 patients by 70% at day 7 compared to placebo. No related hospitalizations or deaths occurred by day 29. Preclinical data suggest the combination can combat resistant SARS-CoV-2 variants. An Emergency Use Authorization application for VIR-7831 has been submitted to the FDA, aiming to expedite its availability for COVID-19 treatment.
Vir Biotechnology and GlaxoSmithKline have applied for Emergency Use Authorization (EUA) from the FDA for VIR-7831, a dual-action monoclonal antibody for adults and adolescents with mild-to-moderate COVID-19 at risk for hospitalization. The application is supported by interim data from the Phase 3 COMET-ICE trial, showing an 85% reduction in hospitalization or death compared to placebo. An Independent Data Monitoring Committee halted further enrollment due to significant efficacy. The companies are also pursuing regulatory discussions in Europe for broader access to this treatment.
Vir Biotechnology and GSK announced that the Independent Data Monitoring Committee recommended stopping the Phase 3 COMET-ICE trial early due to an impressive 85% reduction in hospitalization or death for patients receiving VIR-7831 compared to placebo. Following this, they plan to seek Emergency Use Authorization in the U.S. and other countries. Additionally, in vitro studies show that VIR-7831 retains effectiveness against major COVID-19 variants. The trial involved 583 patients, with ongoing follow-up to gather more data on safety and efficacy.
Vir Biotechnology and GlaxoSmithKline announced an update on their COVID-19 treatment, VIR-7831, during the NIH's ACTIV-3 trial. Although VIR-7831 initially met criteria to advance, concerns regarding its efficacy led to a recommendation to close its enrollment. The Data and Safety Monitoring Board found no safety issues but noted uncertainties about patient benefit. The companies aim to further evaluate VIR-7831's potential while upcoming data from the COMET-ICE trial is anticipated. VIR-7831 is designed to block viral entry and clear infected cells, potentially effective against emerging variants.
Vir Biotechnology (Nasdaq: VIR) reported strong progress in its development pipeline, with six molecules targeting serious infectious diseases. Total revenues for 2020 reached $76.4 million, a significant increase from $8.1 million in 2019, primarily driven by a collaboration with GSK. The company anticipates key data from Phase 3 trials for its monoclonal antibodies against COVID-19 (VIR-7831 and VIR-7832) in early 2021. However, the net loss for Q4 2020 was $105.6 million, up from $63.8 million in Q4 2019, reflecting increased R&D and administrative expenses.
Vir Biotechnology and GlaxoSmithKline have expanded their collaboration to develop monoclonal antibodies for influenza and other respiratory viruses. GSK will invest $120 million and make an upfront payment of $225 million to accelerate research on VIR-2482, an investigational antibody designed for universal prophylaxis against influenza A. This collaboration also includes exploration for additional antibody candidates targeting non-influenza pathogens. The agreement hinges on customary regulatory conditions.
Vir Biotechnology (Nasdaq: VIR) will release its fourth-quarter and full-year financial results for 2020 on February 25, 2021. The corporate update is set to follow after market close and will be available on the company’s website under the Investors section.
Vir is focused on treating serious infectious diseases through innovative immunology technologies and has a pipeline addressing COVID-19, hepatitis B, influenza A, and HIV.
Vir Biotechnology has published new research identifying the N-terminal domain (NTD) of the SARS-CoV-2 spike protein as a target for neutralizing antibodies, with varying efficacy across emerging variants. The findings highlight the NTD's potential role in immune evasion and suggest the need for therapies with high resistance barriers. The investigational antibody VIR-7831, currently in Phase 3 trials, targets a conserved area of the receptor binding domain (RBD) and is designed for effectiveness against SARS-CoV-2 and its variants. Recent studies emphasize the importance of broadening targets to enhance vaccine and therapeutic strategies.
Eli Lilly, Vir Biotechnology, and GlaxoSmithKline have announced a collaboration to study two COVID-19 therapies in low-risk patients. The expanded BLAZE-4 trial will investigate the efficacy of bamlanivimab (700mg) with VIR-7831 (500mg), marking the first time monoclonal antibodies from different companies will be combined. Bamlanivimab is authorized for emergency use against COVID-19, while VIR-7831 is still investigational. The collaboration aims to provide insights into the potential benefits of this combination therapy amidst ongoing COVID-19 challenges.
Eli Lilly (LLY), Vir Biotechnology (VIR), and GlaxoSmithKline (GSK) announced a collaboration to evaluate the combination of their COVID-19 therapies in low-risk patients with mild to moderate COVID-19. The expanded BLAZE-4 trial will assess bamlanivimab (700mg) with VIR-7831 (500mg), both neutralizing antibodies targeting SARS-CoV-2. This marks the first cross-company monoclonal antibody collaboration. Bamlanivimab is authorized for emergency use, while VIR-7831 is investigational. The trial aims to determine if this combination therapy can improve treatment outcomes.