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The launch of Biocon’s Yesafili expands the availability of biosimilar aflibercept 2 mg for patients with age-related macular degeneration and other serious eye conditions in the US.
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AbbVie has received approval from the European Commission (EC) for RINVOQ (upadacitinib; 15 mg and 30 mg, once daily) to treat adults and adolescents aged 12 years and older with severe alopecia areata (AA). Alopecia areata is an autoimmune disorder that causes unpredictable hair loss, ranging from small bald patches on the scalp to complete […]
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Firefly Bio’s Firelink DAC platform will help advance Johnson & Johnson’s strategy to develop targeted therapies for some of the most prevalent and difficult-to-treat solid tumours.
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Chicago-based biopharmaceutical company Meitheal holds exclusive US commercialization rights for Garzulys through its exclusive license agreement with Emerge, the BLA holder.
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Teleflex has received Biologics License Application (BLA) approval for EZPLAZ Freeze Dried Plasma (FDP) from the USFDA.
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Johnson & Johnson’s RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) is currently approved in more than 40 countries, including the US, Europe and Japan, for the subcutaneous treatment of non-small cell lung cancer.
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The framework builds on WHO’s Greener pharmaceuticals’ regulatory highway call to action, launched in 2024.
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Bioequivalent to Merck’s Bridion injection, Sugammadex injection is indicated for the reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide in adults and paediatric patients aged 2 years and older undergoing surgery.
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Spring Fertility launches its new Personalized IVF Calculator, designed to provide fertility patients with more accurate, personalized information about their chances of a successful IVF outcome.
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ELISIO-HX dialyzer, featuring NIPRO’s proprietary membrane technology, enhances middle molecule removal while remaining fully compatible with routine hemodialysis practice.
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