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AUTEL Powers High-Speed EV Charging Station at Bangkok’s Central World
BANGKOK--(BUSINESS WIRE)--AUTEL has partnered with ZEEKR and Evolt to deliver a high-speed EV charging station “ZEEKR Power @centralwOrld” in Bangkok....
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Kaneka Expands Global Reach with i-ED COIL™ Launch in Europe
TOKYO--(BUSINESS WIRE)--Kaneka Corporation (Headquarters: Minato-ku, Tokyo; President: Kazuhiko Fujii) (TOKYO:4118) has begun sales of its i-ED COIL™, a brain aneurysm embolization coil (*1), in Europe as of October. The product obtained EC certification (*2) under an EU Medical Device Regulation (*3) in July and will be distributed primarily in Europe through Kaneka Medical Europe N.V. The i-ED COIL™ provides world-class flexibility, enabled by its specialized wire thickness and structural fea...
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原発性IgA腎症においてメザギタマブ(TAK-079)投与後 18カ月間の腎機能への持続的な影響を示す新たなデータの発表について
大阪(日本)& ケンブリッジ(マサチューセッツ州)--(BUSINESS WIRE)--(ビジネスワイヤ) -- 当社は、このたび、原発性IgA腎症を対象とした、疾患修飾作用が期待される抗CD38モノクローナル抗体メザギタマブ(遺伝子組換え)(TAK-079、以下、メザギタマブ)の皮下投与における第1b相、非盲検、プルーフ・オブ・コンセプト臨床試験の新たな中間データを発表しましたので、お知らせします。本試験のデータから、参加者の腎機能(eGFR)は、メザギタマブ最終投与後、最大18カ月間である96週時点まで安定していることが示唆されました1。この結果は、ヒューストンで開催された米国腎臓学会(ASN)「Kidney Week 2025」(以下、本学会)で発表されました。 IgA腎症は、10歳から30歳の若年層に多く診断される、生涯にわたって進行する自己免疫疾患であり、腎機能に不可逆的な障害を引き起こします2。IgA腎症の病原性機序に作用する根本的な治療法はなく、既存の治療法では、約5人に1人のIgA腎症患者さんが診断から10年以内に腎不全を発症します3。メザギタマブは、病因に関与するガ...
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Foundation for the Development of Western Syria Urges Concrete Commitments from Jolani Regime Ahead of White House Meeting
WASHINGTON--(BUSINESS WIRE)--As President Donald J. Trump prepares to meet Syrian leader Abu Mohammed al-Jolani (also known as Ahmed al-Sharaa) at the White House on Monday, the Foundation for the Development of Western Syria (FDWS) calls on both parties to ensure that this meeting produces tangible commitments that protect Syria’s pluralistic fabric and secure the rights of its vulnerable minorities. For centuries, Syria’s Christian, Alawite, Druze, Kurdish, and other minority communities have...
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Vir Biotechnology Announces AASLD The Liver Meeting® Presentation & New England Journal of Medicine Publication of Phase 2 Data Demonstrating Tobevibart & Elebsiran Combination Deliver High Rates of Undetectable HDV RNA with Favorable Safety Profile
SAN FRANCISCO--(BUSINESS WIRE)--Vir Biotechnology, Inc. (Nasdaq: VIR) today announced that Week 48 endpoint analysis from the Company’s Phase 2 SOLSTICE trial for chronic hepatitis delta (CHD) demonstrated that participants receiving a monthly dose of the combination of tobevibart and elebsiran achieved robust and sustained rates of hepatitis delta virus (HDV) RNA target not detected (TND), including those participants with cirrhosis and high baseline HDV RNA. The combination also showed alanin...
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V.F. Corporation 72 Hour Deadline Alert: Former Louisiana Attorney General And Kahn Swick & Foti, LLC Remind Investors With Losses In Excess Of $100,000 of Deadline in Class Action Lawsuits Against V.F. Corporation - VFC
NEW YORK & NEW ORLEANS--(BUSINESS WIRE)--Kahn Swick & Foti, LLC (“KSF”) and KSF partner, the former Attorney General of Louisiana, Charles C. Foti, Jr., remind investors that they have until November 12, 2025 to file lead plaintiff applications in securities class action lawsuits against V.F. Corporation. (NYSE: VFC), if they purchased or otherwise acquired VFC securities between October 27, 2022 and May 20, 2025, inclusive (the “Class Period”). These actions are pending in the United State...
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Virion Therapeutics Reports Progress Towards HBV Functional Cure with Sustained and Continued HBsAg Declines up to One Year After a Single VRON-0200 Dose From its Phase 1b Study at AASLD’s The Liver Meeting® 2025
PHILADELPHIA--(BUSINESS WIRE)--Virion Therapeutics, LLC, a clinical-stage biotechnology company, developing novel T cell-based immunotherapies that utilize checkpoint modifiers, today announced at AASLD’s The Liver Meeting®, in Washington DC, that a single intramuscular dose of VRON-0200, its novel, first-in-class, immunotherapy for HBV Functional Cure, induced HBV-specific immune activation, restoration, and HBsAg declines, that were sustained and/or continued up to one-year post dosing, in th...
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Merck’s Enlicitide Decanoate, an Investigational Oral PCSK9 Inhibitor, Significantly Reduced LDL-C in Adults with Heterozygous Familial Hypercholesterolemia (HeFH) in Phase 3 CORALreef HeFH Trial
RAHWAY, N.J.--(BUSINESS WIRE)--Merck’s Enlicitide, an Investigational Oral PCSK9 Inhibitor, Significantly Reduced LDL-C in Adults with HeFH in Phase 3 CORALreef HeFH Trial...
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Baxdrostat demonstrated a statistically significant and highly clinically meaningful placebo-adjusted reduction of 14.0 mmHg in 24-hour ambulatory systolic blood pressure in patients with resistant hypertension in the Bax24 Phase III trial
WILMINGTON, Del.--(BUSINESS WIRE)--Positive full results from the Bax24 Phase III trial showed baxdrostat demonstrated a statistically significant and highly clinically meaningful reduction in ambulatory 24-hour average systolic blood pressure (SBP) compared with placebo at 12 weeks. Patients with treatment-resistant hypertension (rHTN) received baxdrostat 2mg or placebo on top of standard of care.1 Efficacy was observed throughout the 24-hour period, including early morning, when patients with...
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Ruszają obrady 26. Zgromadzenia Ogólnego Światowej Organizacji Turystyki w Rijadzie
RIJAD, Arabia Saudyjska--(BUSINESS WIRE)--W dniu dzisiejszym rozpoczęły się obrady 26. Zgromadzenia Ogólnego Światowej Turystyki w Rijadzie, a tym samym po raz pierwszy w regionie Krajów Zatoki Perskiej (ang. GCC), jako największe obrady Zgromadzenia od czasu założenia Światowej Organizacji Turystyki 50 lat temu. W wydarzeniu bierze udział około 160 delegacji z państw członkowskich, w tym ministrów, funkcjonariuszy wyższego szczebla i liderów z całej branży oraz przedstawicieli społeczeństwa ob...