Organon expands TOFIDENCE use to CRS and pediatric COVID-19
The FDA approved the biosimilar for treating CAR T-cell induced CRS and COVID-19 in patients aged 2 and older.
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Global healthcare company focused on women's health
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In short: Organon entered a definitive agreement to be acquired by Sun Pharma for $11.75 billion and received several FDA and EC approvals for its biosimilars.
The FDA approved the biosimilar for treating CAR T-cell induced CRS and COVID-19 in patients aged 2 and older.
POHERDY is the first approved pertuzumab biosimilar in Europe for HER2-positive breast cancer treatments. It expands access via Organon's commercialization rights.
The sale is announced on April 26, 2026.
The 2026 guidelines endorse it as the only steroid-free topical for pediatric atopic dermatitis across severities in children aged 2+.
New activity is brewing for Organon ( ($OGN) ). The company has submitted a Form DEFM14A to the SEC, indicating an upcoming shareholder vote. This...
The investigation concerns whether the Organon Board breached its fiduciary duties to shareholders by failing to conduct a fair process, including whether the proposed transaction...
Organon receives U.S. FDA approval to expand the use of its biosimilar arthritis drug for certain cancer and COVID-19 patients. Concurrently, health systems face issues...
Organon closes an indication gap with Tofidence, but subcutaneous availability and market share remain areas where its tocilizumab biosimilar still lags behind.
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