We are pleased to share that our partner Takeda has received positive CHMP Opinion for a new treatment for adults with previously treated metastatic #ColorectalCancer #mCRC throughout the European Union, Norway, Liechtenstein and Iceland. Learn More:https://lnkd.in/gnwjpgCR
HUTCHMED
Biotechnology Research
Building a global science-focused biopharma from an established base in China.
About us
HUTCHMED (Nasdaq/AIM:HCM; HKEX:13) is an innovative, commercial-stage, biopharmaceutical company. It is committed to the discovery and global development and commercialization of targeted therapies and immunotherapies for the treatment of cancer and immunological diseases. A dedicated organization of over 1,300 personnel has advanced ten cancer drug candidates from in-house discovery into clinical studies around the world, with its first three oncology drugs now approved and launched. For more information, please visit: www.hutch-med.com or follow us here on LinkedIn.
- Website
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https://www.hutch-med.com
External link for HUTCHMED
- Industry
- Biotechnology Research
- Company size
- 5,001-10,000 employees
- Headquarters
- Hong Kong
- Type
- Public Company
- Founded
- 2000
- Specialties
- Pharmaceutical, Biopharmaceutical, Innovation, Research and Development, Oncology, Hematology, Immunology, Inflammation, Cancer, and Targeted Therapy
Locations
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Primary
Metropolis Tower, 10 Metropolis Drive, Hung Hom
Level 18
Hong Kong, HK
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917 Halei Road, Building 4, Zhangjiang Hi-Tech Park
Pudong, Shanghai 201203, CN
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25A Vreeland Road
Suite 304
Florham Park, NJ 07932, US
Employees at HUTCHMED
Updates
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New and updated data from several studies of compounds discovered by HUTCHMED will be presented at the upcoming American Association of Cancer Research Annual Meeting 2024 #AACR24 , taking place on April 5-10, 2024 in San Diego, California. https://lnkd.in/gMNzSavN
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We are happy to share that, in collaboration with Innovent Biologics, the New Drug Application (NDA) for the combination of fruquintinib and sintilimab for the treatment of patients with advanced endometrial cancer has been accepted and granted priority review by the China National Medical Products Administration. https://lnkd.in/ghYRFhFr
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The supplemental New Drug Application (sNDA) for savolitinib, in adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with MET exon 14 skipping alteration, has been accepted for review by the China National Medical Products Administration. If approved, the new label indication for savolitinib will be expanded to include treatment-naive patients in China. https://lnkd.in/guMVw_nH
HUTCHMED Announces Savolitinib sNDA Accepted in China for Treatment-Naïve or Previously Treated Patients with Locally Advanced or Metastatic
https://www.hutch-med.com
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We are pleased to announce that we have initiated the registration stage of the Phase II/III clinical trial of sovleplenib in adult patients with warm antibody autoimmune hemolytic anemia (“wAIHA”) in China. wAIHA is an autoimmune disorder that can lead to anemia and has limited treatment options. This follows positive data from the proof-of-concept Phase II stage of the trial and subsequent consultation with the China National Medical Products Administration. If positive, the data from the trial may be used to support a future New Drug Application filing. https://lnkd.in/g2NfJt-k
HUTCHMED Initiates Registration Stage of the ESLIM-02 Phase II/III Trial of Sovleplenib for Warm Antibody Autoimmune Hemolytic Anemia in Chi
https://www.hutch-med.com
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2023 was an important year for HUTCHMED. We made significant progress and executed against our commitment to bring our innovative medicines to patients worldwide, while remaining dedicated to becoming a self-sustaining business. Today, we are happy to report our 2023 Full Year Financial Results: https://lnkd.in/deweff_c
HUTCHMED Reports 2023 Full Year Results and Provides Business Updates
https://www.hutch-med.com
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We will be announcing our 2023 final results on Wednesday, February 28, 2024. Analysts and investors are invited to join a conference call and audio webcast presentation with Q&A, conducted by HUTCHMED management. https://lnkd.in/gbTek2a7
HUTCHMED to Announce 2023 Final Results
https://www.hutch-med.com
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Data from FRUTIGA, HUTCHMED’s Phase III trial of fruquintinib in combination with paclitaxel for the treatment of second-line advanced gastric cancer in China, were presented at the American Society of Clinical Oncology (ASCO) Plenary Series Session on February 6, 2024. Follow the link for the full presentation: https://lnkd.in/gjPwBwTN
ASCO Plenary Series Program
old-prod.asco.org
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