As concern mounted about the regulatory chances for Eli Lilly and Company/Innovent Biologics, Inc.’s PD-1 inhibitor sintilimab, Lilly tried to tap into the argument that more PD-1/L1 inhibitors could drive down costs for a class of drugs seeing wider and wider use. But a negative vote from the US Food and Drug Administration’s Oncologic Drugs Advisory Committee (ODAC) suggests that the entire wave of China-developed PD-1/L1 inhibitors will face the same regulatory obstacles.
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