April 5 (Reuters) - The U.S. Food and Drug Administration on Friday allowed the expanded use of Johnson & Johnson and Legend Biotech's Carvykti cell therapy as an earlier treatment for patients with a type of blood cancer. (Reporting by Disha Mishra in Bengaluru; Editing by William Mallard)
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45.69 USD | -0.07% | -0.65% | -24.16% |
Apr. 23 | Genscript Biotech Unit Gets Approval for Blood Cancer Drug by European Commission | MT |
Apr. 22 | Legend Biotech's Carvykti Gets European Commission Approval for Treatment of Blood Cancer | MT |
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150 USD | +0.70% | -0.01% | 358B | ||
45.69 USD | -0.07% | -0.65% | 8.32B | ||
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-7.93% | 17.19B | |
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