Tafasitamab has been approved for marketing in Hong Kong and approval for use in Bo’ao and the Greater Bay Area. In Mainland China,patient enrollment of the registrational trial of tafasitamab in combination with lenalidomide was completed in China. The Company expects to submit the biologics license application (BLA) in the second quarter of 2024.
Thanks to the early access program in Bo’ao, the first prescription of tafasitamab in combination with lenalidomide was filed in July, 2022, bringing hope to DLBCL patients in China.