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» FDA clears IND for NBL-020 for advanced solid tumors
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Immuno-oncology
FDA clears IND for NBL-020 for advanced solid tumors
Dec. 23, 2022
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The FDA has cleared an IND for a clinical trial in the U.S. of NBL-020, a fully human antibody drug independently developed by CSPC Pharmaceutical Group Ltd.'s subsidiary Novarock Biotherapeutics Ltd., for the treatment of advanced solid tumors.
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