Henlius Biotech Gets US FDA Nod for Breast Cancer Drug's Biologics License Application

MT Newswires Live

11/14

Shanghai Henlius Biotech (HKG:2696) obtained approval for the biologics license application of POHERDY injection for intravenous use from the US Food and Drug Administration (FDA), a Friday Hong Kong bourse filing said.

The approved indications include use in combination with trastuzumab and chemotherapy in the treatment of adults with breast cancer.

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