HUTCHMED Announces European Commission Approval for FRUZAQLA® (fruquintinib) Received by Takeda
HUTCHMED (China) Limited - American Depositary Shares (HCM)
NASDAQ:AMEX Investor Relations:
chi-med.com/investors/information-for-shareholders
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Source: GlobeNewswire
— Approval for previously treated metastatic colorectal cancer based on results from positive, global, Phase III FRESCO-2 Trial — — FRUZAQLA® (fruquintinib) is the first novel targeted therapy in the EU for metastatic colorectal cancer regardless of biomarker status in over a decade — HONG KONG, SHANGHAI and FLORHAM PARK, N.J., June 21, 2024 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited (“HUTCHMED”) (Nasdaq/AIM:HCM; HKEX:13) today announces that its partner Takeda (TSE:4502/?NYSE:TAK) has received notification from the European Commission (“EC”) that it has approved FRUZAQLA® (fruquintinib) as a monotherapy indicated for the treatment of adult patients with metastatic colorectal cancer (“CRC”) who have been previously treated with available standard therapies, including fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapies, anti-VEGF agents, and anti-EGFR agents, and who have progressed on or are intolerant to treatment with either trifluridine-tipiracil or regorafen
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News
- HUTCHMED to Announce 2024 Half-Year Financial ResultsGlobeNewswire
- Save the Date: HUTCHMED to Present R&D Updates on July 9, 2024 [Yahoo! Finance]Yahoo! Finance
- Save the Date: HUTCHMED to Present R&D Updates on July 9, 2024GlobeNewswire
- HUTCHMED Announces European Commission Approval for FRUZAQLA® (fruquintinib) Received by Takeda [Yahoo! Finance]Yahoo! Finance
- HUTCHMED Highlights Publication of Phase III ESLIM-01 Results in The Lancet Haematology [Yahoo! Finance]Yahoo! Finance
HCM
Sec Filings
- 6/28/24 - Form 6-K
- 6/28/24 - Form F-3ASR
- 6/26/24 - Form 6-K
- HCM's page on the SEC website