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Day: January 25, 2026

FDA Accepts LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease under Priority Review

If approved, LEQEMBI IQLIK would be the first and only anti-amyloid treatment to offer at-home injection options for initiation and maintenance dosing for this progressive, relentless disease FDA action date set for May 24, 2026 TOKYO and CAMBRIDGE, Mass., Jan. 25, 2026 (GLOBE NEWSWIRE) — Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts, CEO: Christopher A. Viehbacher, “Biogen”) announced today that the U.S. Food and Drug Administration (FDA) has accepted for review Eisai’s Supplemental Biologics License Application (sBLA) for lecanemab-irmb (U.S. brand name: LEQEMBI®) subcutaneous autoinjector (SC-AI), LEQEMBI IQLIK, as a weekly starting dose. LEQEMBI is indicated for the treatment of Alzheimer’s disease (AD) in patients with Mild Cognitive...

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Data at 2026 Boswick Burn & Wound Symposium highlight first integrated use of AVITA Medical technologies

First surgeon-reported case using RECELL®, PermeaDerm®, and Cohealyx™ together in a single care pathwayNew clinical and tissue-level data on PermeaDerm and Cohealyx highlight wound bed preparation and readiness for closureRECELL analyses show consistent trends in healing, reduced complications, and shorter hospital stays across studies and real-world registry dataVALENCIA, Calif., Jan. 25, 2026 (GLOBE NEWSWIRE) — AVITA Medical®, Inc. (ASX: AVH, NASDAQ: RCEL), a leading therapeutic acute wound care company delivering transformative solutions, today announced data from 19 scientific abstracts, including 14 podium presentations, at the 2026 Boswick Burn & Wound Symposium. The presentations include the first surgeon-reported integrated use of all three AVITA Medical technologies – RECELL, PermeaDerm, and Cohealyx...

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Baker Hughes Announces Fourth-Quarter and Full-Year 2025 Results

Fourth-quarter highlightsOrders of $7.9 billion, including $4.0 billion of IET orders. Record RPO of $35.9 billion, including record IET RPO of $32.4 billion. Revenue of $7.4 billion, flat year-over-year. Attributable net income of $876 million. GAAP diluted EPS of $0.88 and adjusted diluted EPS* of $0.78. Adjusted EBITDA* of $1,337 million, up 2% year-over-year. Cash flows from operating activities of $1,662 million and free cash flow* of $1,341 million.Full-year highlightsOrders of $29.6 billion, including record $14.9 billion of IET orders. Revenue of $27.7 billion, flat year-over-year. Attributable net income of $2,588 million. GAAP diluted EPS of $2.60 and adjusted diluted EPS* of $2.60. Adjusted EBITDA* of $4,825 million, up 5% year-over-year. Cash flows from operating activities of $3,810 million and free cash flow* of $2,732...

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