HUTCHMED Announces China Approval for ORPATHYS® and TAGRISSO® Combination in Lung Cancer
The healthcare company has received approval in China for a new lung cancer treatment combination.
The healthcare company has received approval in China for a new lung cancer treatment combination.
The healthcare company has granted share options and LTIP awards to its executive team as part of its compensation and retention strategy.
The biopharmaceutical company has announced that its NDA for a combination therapy to treat advanced renal cell carcinoma has been accepted for review, marking a key milestone in bringing this potential new treatment option to patients.
The biopharmaceutical company has announced positive results from a Phase III study of its savolitinib and osimertinib combination therapy for NSCLC patients.
The biopharmaceutical company HUTCHMED announces that new data from several studies of its compounds will be presented at the upcoming ASCO Annual Meeting.
The biopharmaceutical company HUTCHMED announces data from several studies of its compounds, including savolitinib, fruquintinib and surufatinib, to be presented at the upcoming AACR Annual Meeting 2025.
The biopharmaceutical company has completed enrollment for a Phase II study evaluating its drug savolitinib in treating gastric cancer patients with MET amplification.
The biopharmaceutical company has released its 2024 Annual Report and announced the details of its upcoming Annual General Meeting.
The biopharmaceutical company receives conditional approval from China's NMPA for its TAZVERIK® treatment for relapsed or refractory follicular lymphoma, marking an important milestone in expanding its product portfolio.
The healthcare company announces the retirement of two long-serving independent directors from its board.