Communiqués HUTCHMED (China) Limited

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KYG4672N1198

Produits pharmaceutiques

Temps Différé London S.E. 16:41:32 16/06/2026 Varia. 5j. Varia. 1 janv.
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Communiqués

05/03 HUTCHMED Initiates Global Trial of PI3K/PIKK-EGFR ATTC Candidate HMPL-A580 in Patients with Solid Tumors AQ
07/01 HUTCHMED China : English Presentation PU
24/04/25 HUTCHMED Highlights Data to be Presented at AACR Annual Meeting 2025 AQ
22/04/25 HUTCHMED Completes Patient Enrollment of a Phase II Registration Study of Savolitinib in Gastric Cancer in China AQ
24/03/25 HUTCHMED Announces NMPA Conditional Approval for TAZVERIK for the Treatment of Relapsed or Refractory Follicular Lymphoma AQ
20/03/25 HUTCHMED Highlights Savolitinib SAVANNAH Phase II and Other Data at European Lung Cancer Congress 2025 AQ
06/03/25 HUTCHMED Announces that it has Completed Enrollment of a Phase II Registration Study of Fanregratinib (HMPL-453) for Intrahepatic Cholangiocarcinoma in China AQ
14/01/25 HUTCHMED Announces NMPA Full Approval for ORPATHYS® (savolitinib) in China for Patients with Locally Advanced or Metastatic MET Exon 14 NSCLC AQ
02/01/25 HUTCHMED China : Announces US$608 million Divestment of Non Core Joint Venture Form 6 K PU
02/01/25 HUTCHMED Announces NDA Acceptance in China with Priority Review Status for ORPATHYS® and TAGRISSO® Combination in Lung Cancer Patients with MET amplification After Progression on First-Line EGFR Inhibitor Therapy AQ
13/12/24 HUTCHMED China : to Receive Milestone Payment from Takeda following First European Reimbursement for FRUZAQLA® (fruquintinib) Form 6 K PU
12/12/24 HUTCHMED China : Announces Breakthrough Therapy Designation in China for ORPATHYS® and TAGRISSO® Combination in Certain Lung Cancer Patients After Disease Progression on EGFR Inhibitor Therapy Form 6 K PU
12/12/24 HUTCHMED Announces Breakthrough Therapy Designation in China for ORPATHYS® and TAGRISSO® Combination in Certain Lung Cancer Patients After Disease Progression on EGFR Inhibitor Therapy AQ
03/12/24 HUTCHMED China : and Innovent Jointly Announce NMPA Conditional Approval for ELUNATE® (Fruquintinib) in Combination with TYVYT® (Sintilimab Injection) for the Treatment of Advanced Endometrial Cancer Form 6 K PU
29/11/24 HUTCHMED China : Announces Continued Inclusion of ORPATHYS® (savolitinib) in the National Reimbursement Drug List in China at Current Terms Form 6 K PU
22/11/24 HUTCHMED China : Announces Launch by Takeda of FRUZAQLA® (fruquintinib) in Japan Form 6 K PU
22/11/24 HUTCHMED Announces Launch by Takeda of FRUZAQLA® (fruquintinib) in Japan AQ
20/11/24 HUTCHMED China : Announces Appointment of Independent Non executive Director and Member of Board Committee Form 6 K PU
20/11/24 HUTCHMED Announces Appointment of Independent Non-executive Director and Member of Board Committee  AQ
06/11/24 HUTCHMED China : Highlights Clinical Data to be Presented at the 2024 ASH Annual Meeting and the 2024 ESMO Asia Congress Form 6 K PU
06/11/24 HUTCHMED Highlights Clinical Data to be Presented at the 2024 ASH Annual Meeting and the 2024 ESMO Asia Congress AQ
31/10/24 HUTCHMED to Receive First Commercial Milestone Payment Following Over US$200 Million in FRUZAQLA® (fruquintinib) Sales by Takeda AQ
16/10/24 HUTCHMED China : Announces that TAGRISSO® plus ORPATHYS® demonstrated high, clinically meaningful response rate in lung cancer patients with high levels of MET overexpression and/or amplification in SAVANNAH Phase II trial Form 6 K PU
16/10/24 HUTCHMED Announces that TAGRISSO® plus ORPATHYS® demonstrated high, clinically meaningful response rate in lung cancer patients with high levels of MET overexpression and/or amplification in SAVANNAH Phase II trial AQ
09/09/24 HUTCHMED Highlights Clinical Data to be Presented at ESMO Congress 2024 and the 2024 World Conference of Lung Cancer AQ
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