Story · Medicine & Biotech
STAT+: FDA approves novel Bayer drug to reduce recurrence of stroke
8 outlets · first reported by FDA Drug Safety / Drugs feed on · latest · 96 hours of coverage · 5 countries
The Food and Drug Administration on Monday approved Bayer’s drug to reduce recurrence of stroke, making available the first in a novel class of medications that hold the promise of preventing blood clots more safely. Many blood thinners aren’t used in this setting due to their increased risk of… (STAT News)
Coverage, in order
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FDA Approves First Factor Xla Inhibitor to Help Prevent Stroke in Certain Adults at High Risk
FDA today approved Sunharbo (asundexian) 50 mg tablets, the first factor XIa (FXIa) inhibitor for use in combination with antiplatelet therapy to reduce the risk of stroke in adults following a recent mild-to-moderate non-cardioembolic ischemic stroke or a high-risk transient ischemic attack.
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STAT+: FDA approves novel Bayer drug to reduce recurrence of strokeThe Food and Drug Administration on Monday approved Bayer’s drug to reduce recurrence of stroke, making available the first in a novel class of medications that hold the promise of preventing blood clots more safely. Many blood thinners aren’t used in this setting due to their increased risk of…
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Bayer bags FDA green light for stroke drug Sunharbo
Bayer bags FDA green light for stroke drug Sunharbo Phil.Taylor Tue, 10/11/2026 - 09:36
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FDA approves a new drug against recurrent strokeFDA одобри нов медикамент срещу повторен инсултTablets cut recurrent ischaemic stroke risk by 26%.Таблетките намаляват с 26% риска от повторен исхемичен инцидент, съобщиха от Агенцията
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FDA Approves First Factor Xla Inhibitor to Help Prevent Stroke in Certain Adults at High RiskThe U.S. Food and Drug Administration has approved Sunharbo (asundexian) 50 mg tablets, the first factor XIa (FXIa) inhibitor for use in combination with antiplatelet therapy to reduce the risk of stroke in adults following a recent mild-to-moderate non-cardioembolic ischemic stroke (a stroke…
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FDA Approves First-in-Class Bayer Drug for Reducing the Risk of StrokeBayer’s asundexian, brand name Sunharbo, is the first FDA-approved drug in a new class cardiovascular medicines Approval of the once-daily pill covers secondary stroke prevention in adults.
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FDA approves first-in-class drug for secondary stroke preventionAn FDA statement called the new approval of Bayer's asundexian a "meaningful advance for patients and healthcare providers seeking a new option for secondary stroke prevention."
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FDA Approves First Drug to Treat Adults with Primary Membranous Nephropathy
FDA approved Gazyva (obinutuzumab) injection to induce remission of proteinuria (protein in the urine) in adults with primary membranous nephropathy at risk of disease progression.
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