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The US Food and Drug Administration (FDA) has granted accelerated approval for Regeneron Pharmaceuticals’ Lynozyfic ...
According to Regeneron, the drug is a bispecific antibody that binds to B-cell maturation antigen (BCMA) on cancerous plasma cells and CD3 on T cells, directing the immune system to attack and destroy ...
5d
The Print on MSNGovt considers low-dose emicizumab for haemophilia, trial finds it more effective than existing treatmentMiracle drug’ can cost Rs 13 lakh for haemophilia A patient annually, but reduced dose found efficacious & cost-effective in ...
A once-a-day pill that could completely revolutionise the treatment of Alzheimer’s disease has reached a significant ...
The Global Bioinformatics Market is expected to grow at a rate of 13-14% by 2029. The rising government initiatives and ...
FDA's plan to phase out animal testing may hurt Charles River's revenues. The DCF model suggests that CRL presents an ...
Riliprubart granted orphan drug designation in Japan for chronic inflammatory demyelinating polyneuropathy Two phase 3 studies are currently underway testing riliprubart in people with CIDP as a ...
Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval for Lynozyfic™ (linvoseltamab-gcpt) to treat adult ...
News Commentary Issued on behalf of Avant Technologies Inc. VANCOUVER, BC, June 30, 2025 /CNW/ — Several experts are seeing that value of AI’s total overhaul of ...
Phase 1b study supports proof-of-concept in DOK7 congenital myasthenic syndromes Advancing ARGX-119 further validates strong track record of Immunology Innovation Program (IIP), argenx's collaborative ...
A revolutionary new type of "Trojan horse" cancer therapy, now being deployed under the National Health Service in England, ...
Alphabet-founded biotech Calico Life Sciences has struck an exclusive licensing agreement with Chinese drugmaker Mabwell (SHA ...
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