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Stock impact report

FDA Approves Genentech's TNKase® in Acute Ischemic Stroke in Adults [Yahoo! Finance]

ROCHE HOLDING LTD S/ADR (RHHBY) 
NASDAQ:AMEX Investor Relations: roche.com/investors.htm
Company Research Source: Yahoo! Finance
– Single five-second intravenous bolus provides faster and simpler administration than the approved standard-of-care – – Genentech has developed the only two FDA-approved medicines to treat acute ischemic stroke, TNKase and Activase ® (alteplase) – SOUTH SAN FRANCISCO, Calif., March 03, 2025 BUSINESS WIRE )--Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced that the U.S. Food and Drug Administration (FDA) has approved TNKase ® (tenecteplase), a thrombolytic or clot-dissolving agent, for the treatment of acute ischemic stroke (AIS) in adults. This approval of TNKase marks Genentech's second approval for stroke, reinforcing the company's long-standing dedication to advancing stroke care as the developer of the only two FDA-approved medicines for AIS, TNKase and Activase ® (alteplase). TNKase is delivered as a single five-second intravenous (IV) bolus, a faster and simpler administration compared to the standard-of-care, Activase, which is admini Show less Read more
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