JNJ Anssen Submits Supplemental Biologics License Application To U.S. FDA Seeking Approval Of CARVYKTI For Earlier Treatment Of Patients With Relapsed Or Refractory Multiple Myeloma
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JNJ's Anssen has submitted a supplemental Biologics License Application to the U.S. FDA, seeking approval for CARVYKTI to treat patients with relapsed or refractory multiple myeloma at an earlier stage.
June 06, 2023 | 8:32 pm
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JNJ's Anssen seeks FDA approval for CARVYKTI to treat relapsed or refractory multiple myeloma patients earlier, potentially expanding the drug's market.
JNJ's Anssen is seeking FDA approval for CARVYKTI to treat patients with relapsed or refractory multiple myeloma at an earlier stage. If approved, this could expand the drug's market and potentially increase JNJ's revenues. The news is directly related to JNJ and has a high importance for investors, as it could impact the company's financial performance.
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