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Press releaseGlobeNewswire· April 13, 2026

Press Release: Sanofi and Regeneron’s Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria

View original at globenewswire.com
Press Release: Sanofi and Regeneron’s Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria Sanofi and Regeneron’s Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria Approval in CSU for chi…
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  • Dupixent provides a first-of-its kind approach to addressing chronic spontaneous urticaria in young children by inhibiting signaling of IL-4 and IL-13, two key drivers of type 2 inflammation

    60% confidence
  • IL-4 and IL-13 are two of the key and central drivers of type 2 inflammation that plays a major role in multiple related and often co-morbid diseases

    60% confidence
  • Previous treatment options for young children with chronic spontaneous urticaria left many patients with uncontrolled disease where the unpredictable appearance of itch and hives continued to disrupt their daily lives

    60% confidence
  • Dupixent has the potential to become the new standard of care for young children with CSU who remain symptomatic despite other available treatments

    60% confidence
  • This approval demonstrates our commitment to extending the value of Dupixent to all who may benefit, including young children

    60% confidence
  • Dupixent is the most widely used innovative branded antibody medicine in the world

    60% confidence
  • This fourth approval for young children with chronic diseases driven in part by type 2 inflammation brings Dupixent's proven efficacy and long-term safety profile to yet another vulnerable population in need

    60% confidence

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Q4 2026 Biotech Catalyst Window: ESMO Data, the Ivonescimab PDUFA and Small-Cap Delistings
Mid-October to November 2026 is a dense catalyst period for clinical-stage biotech. Positive late-stage readouts (ALOFT-IPF, TELIGAN, MIUDELLA, the duvakitug extension) and the ESMO 2026 presentations lead up to the FDA's 14 November PDUFA date for the ivonescimab BLA. At the opposite end of the market, Spago Nanomedical is moving to delist from Nasdaq First North, which shows how hard it is for micro-cap developers to fund themselves. Value is concentrating in companies with late-stage data and near-term regulatory outcomes.
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Ford Motor Company
Both facts give cash for Ford Motor Company at the same point in time (2025-12-31; FY 2025 year-end and Q4 2025 year-end are the same date). Both are labelled USD, but the values are 23,356,000,000 and 23.356, which cannot both be true in USD. The two numbers agree once the second is read as billions (23.356 bn = 23,356,000,000), so the economic content is consistent and the conflict is a unit/scale error in the Q4 2025 record. The period is not the reason for the conflict: a Q4 and an FY figure at the same year-end date should match.
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