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No USFDA approval for AstraZeneca's treatment for chronic nasal condition
The London-listed drugmaker said the U.S. Food and Drug Administration (FDA) had issued a complete response letter following AstraZeneca's application to extend use of the treatment and requested additional clinical data from it.
New Delhi: - AstraZeneca Plc said on Monday the U.S. drug regulator declined to approve its asthma medicine, Fasenra, for treatment of chronic rhinosinusitis with nasal polyps, a condition characterised by benign growths that cause pain and stuffiness.
The London-listed drugmaker said the U.S. Food and Drug Administration (FDA) had issued a complete response letter following AstraZeneca's application to extend use of the treatment and requested additional clinical data from it.
Fasenra was AstraZeneca's first respiratory biologic and raked in $1.26 billion in sales in 2021, jumping 33% from the previous year. It belongs to a class of medicines called monoclonal antibodies and is used against severe asthma.
The treatment rivals GlaxoSmithKline's Nucala and Teva's Cinqair from the same drug class, while AstraZeneca has also developed a newer medicine, Tezspire, with Amgen (AMGN.O) which would compete with Fasenra.
An approval would have challenged Sanofi's Dupixent and Novartis's Xolair, the two biologic respiratory drugs that have so far won approval to treat chronic rhinosinusitis with nasal polyposis.
The setback for AstraZeneca's Fasenra comes after the drugmaker said on Friday the FDA had approved its and Merck's (MRK.N) cancer drug, Lynparza, as a treatment for patients with early-stage breast cancer with certain mutations.
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AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines in Oncology, Rare Diseases, and BioPharmaceuticals, including Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Based in Cambridge, UK, AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide.
Read Also - AstraZeneca and Merck's Lynparza gets USFDA nod
Medical Dialogues Bureau consists of a team of passionate medical/scientific writers, led by doctors and healthcare researchers. Our team efforts to bring you updated and timely news about the important happenings of the medical and healthcare sector. Our editorial team can be reached at editorial@medicaldialogues.in.