
Danish drugmaker Novo Nordisk (NOV: N) has asked the US Food and Drug Administration regulator to assess a stronger 7.2 mg version of its obesity drug Wegovy (semaglutide) under the FDA Commissioner's national priority voucher scheme, potentially clearing the way for a rapid decision. The filing targets adults needing chronic weight-management support.
“Our pipeline is rapidly expanding to meet the needs of people living with obesity, and this submission—under the FDA’s new expedited review program—marks an exciting step forward,” said Anna Windle, senior vice president for clinical development, medical and regulatory affairs at Novo Nordisk.
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