Reported Earlier, HUTCHMED Gains China Approval For ATLED (Fanregratinib) As Confirmatory Phase IIIb Trial Enrollment Continues For FGFR2-Positive Cholangiocarcinoma

HUTCHMED Announces NMPA Approval for ATLED® (Fanregratinib) for the Treatment of Patients with FGFR2-Fusion/Rearrangement Intrahepatic Cholangiocarcinoma

HUTCHMED received conditional approval from China's NMPA for ATLED® (fanregratinib), a selective FGFR 1/2/3 inhibitor, for treating advanced intrahepatic cholangiocarcinoma with FGFR2 fusions/rearrangements in previously treated patients. The Phase II trial demonstrated an objective response rate of 42.5%, median PFS of 6.9 months, and median OS of 16.6 months, addressing a significant therapeutic gap in this aggressive cancer type.

AstraZeneca Reports Mixed Lung Cancer Trial Outcomes From Three Pivotal Studies

AstraZeneca reports mixed lung cancer trial data, highlighting successes for Tagrisso and Enhertu while halting a volrustomig study.

HUTCHMED shares are trading higher after the company announced high-level results from the SAFFRON Phase III trial.