
On Thursday, the Oncology Drug Advisory Committee (ODAC), an advisory panel of the US Food and Drug Administration, voted 14 to 1 that Eli Lilly (NYSE; LLY) and Innovent Biologics (HKEX: 01801) should conduct more trials of their anti-PD-1 antibody sintilimab in order to win approval for the drug in the USA.
The vote come a day after FDA staff released pre-meeting papers that concluded the Chinese study used to support the drug's administration in first-line non-small-cell lung cancer (NSCLC) had several shortcomings and its results were not applicable to US patients.
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