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Race Oncology has activated its first Hong Kong clinical site for the Phase 1 trial of RC220 in combination with doxorubicin in advanced solid tumors. Screening has commenced, with the first Hong Kong patient expected to begin treatment this month. Two patients have already been treated with RC220 in Australia, and recruitment is expected to accelerate as new sites open in Hong Kong and South Korea.
Zai Lab Limited (NASDAQ: ZLAB; HKEX: 9688) announced that the Hong Kong Department of Health has approved TIVDAK (tisotumab vedotin-tftv) for the treatment of adult patients with recurrent or metastatic cervical cancer with disease progression on or after chemotherapy [1]. This approval marks an important milestone for Zai Lab, strengthening its Women’s franchise in Greater China. TIVDAK is the first antibody-drug conjugate (ADC) therapy in cervical cancer, offering a clinically meaningful survival benefit to patients [1].
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