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Press releaseGlobeNewswire· March 24, 2026

Communiqué de presse : Dupixent, développé par Sanofi et Regeneron, a été approuvé au Japon comme premier médicament ciblé pour le traitement des adultes atteints de pemphigoïde bulleuse

View original at globenewswire.com
Communiqué de presse : Dupixent, développé par Sanofi et Regeneron, a été approuvé au Japon comme premier médicament ciblé pour le traitement des adultes atteints de pemphigoïde bulleuse Dupixent, développé par Sanofi et Regeneron, a été approuvé au Japon comme premier médicament ciblé pour le traitement des adultes at…
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  • Dupixent has been approved in Japan as the first targeted medication for treatment of adults with bullous pemphigoid

    60% confidence
  • Dupilumab has been studied in more than 60 clinical studies involving more than 12,000 patients with various chronic diseases partly due to type 2 inflammation

    60% confidence
  • Dupixent is a fully human monoclonal antibody that inhibits IL-4 and IL-13 pathway signaling and is not an immunosuppressant

    60% confidence
  • More than four times as many patients treated with Dupixent achieved sustained disease remission compared to placebo (18% vs. 4%; p=0.0250) at week 36

    60% confidence
  • More than 1.4 million patients are treated with Dupixent worldwide

    60% confidence
  • Dupixent has received regulatory authorizations in more than 60 countries for one or more indications

    60% confidence
  • Bullous pemphigoid is the seventh approved indication for Dupixent in Japan

    60% confidence
  • Treatment-related adverse events occurred in 26% of patients treated with Dupixent and in 15% of patients on placebo, with conjunctivitis being the most frequently reported at 4%

    60% confidence
  • Dupixent's development program has shown significant clinical benefit and reduction in type 2 inflammation in phase 3 studies, establishing that IL-4 and IL-13 are two key and central factors of type 2 inflammation

    60% confidence

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Late-2026 Biotech Catalyst Season: FDA Decisions and Pivotal Readouts Converge Across Oncology, Hepatology and Cardiometabolic
Mid-November 2026 is dense with scheduled biotech catalysts. The ivonescimab BLA PDUFA date is 2026-11-14, the lorundrostat PDUFA date is 2026-12-22, and Phase 3 ECLIPSE hepatitis delta data are due in Q1 2027. Alongside these, siRNA and antibody programs (plozasiran, elebsiran/tobevibart, ianalumab, nipocalimab) reported or presented data at AHA, AASLD, ACR and ASH, while Oryzon advanced iadademstat in AML with Spanish trial authorizations and a planned ALICE-3 Phase III. Late-stage data and regulatory milestones are driving the sentiment. A planned delisting (EGM 2026-11-19, application 2027-01-25) is a separate corporate-structure event with no clear link to the rest.
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High probability of expanded label indications, additional combination approvals, and competitive positioning strength in follicular lymphoma market. Predicts positive commercial uptake and potential accelerated review for related indications.
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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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