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AEON Biopharma Reports Full Year 2025 Financial Results and Highlights Positive Comparative Analytical Results and FDA Feedback for ABP-450 Biosimilar Prog
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Teva’s biosimilar, PONLIMSI™, is now FDA-approved across all indications of the reference product, Prolia® (denosumab), to treat a variety of debilitating bone conditions.Teva’s proposed biosimilar...
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AEON Biopharma Announces FDA Feedback Following BPD Type 2a Meeting for the ABP-450 Biosimilar Program
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AEON Biopharma Abstract Accepted for Presentation at 2026 American Academy of Neurology (AAN) Annual Meeting
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Dublin, Feb. 27, 2026 (GLOBE NEWSWIRE) -- The "Generic and Biosimilar Pharmaceuticals - Industry Report" report has been added to ResearchAndMarkets.com's offering. Using an exclusive...
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Dublin, Feb. 20, 2026 (GLOBE NEWSWIRE) -- The "State of the Life Sciences Industry - Fourth Quarter Review" has been added to ResearchAndMarkets.com's offering. The latest quarterly research...
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Dublin, Feb. 16, 2026 (GLOBE NEWSWIRE) -- The "India Biosimilars Market: Industry Trends and Global Forecasts - Distribution by Drug Class, Therapeutic Area, Type of Manufacturer, Distribution...
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Dublin, Feb. 04, 2026 (GLOBE NEWSWIRE) -- The "Oncology Biosimilars Market" report has been added to ResearchAndMarkets.com's offering.The global market for oncology biosimilars is estimated to...
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AEON Biopharma Reports BPD Type 2a Meeting with FDA and Shareholder Approval of the November Transactions
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ACCRA, Ghana and KIGALI, Rwanda, Jan. 13, 2026 (GLOBE NEWSWIRE) -- Bio Usawa Biotechnology Ltd. (Bio Usawa, Inc.) today announced that the Ghana Food and Drugs Authority (Ghana FDA) has approved...