Hutchmed (China) Limited Clinical Data to be Presented at ESMO 2023

TIDMHCM

Hutchmed (China) Limited

16 October 2023

Press Release

HUTCHMED Highlights Clinical Data to be Presented at ESMO Congress 2023

Hong Kong, Shanghai & Florham Park, NJ - Monday, October 16, 2023: HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM: HCM; HKEX: 13) today announces that new and updated clinical data from several ongoing studies of fruquintinib, in combination with chemotherapies and/or immunotherapies, will be presented at the upcoming European Society for Medical Oncology ("ESMO") Congress 2023, taking place on October 20-24, 2023 in Madrid, Spain.

Details of the presentations are as follows:

 
             Abstract title                   Presenter / Lead           Presentation 
                                                    author                  details 
========================================  =========================  ==================== 
 
 SPONSORED STUDY 
Fruquintinib plus Sintilimab in           Xiaoli Wei, Harbin         1519P 
 patients with either treatment            Medical University         Poster presentation 
 naïve or previously treated          Cancer Hospital,           (Oesophagogastric 
 advanced gastric or gastroesophageal      Harbin, China              cancer) 
 junction adenocarcinoma: results                                     Monday, October 
 from a multicenter, single-arm                                       23, 2023 
 phase Ib/II study 
========================================  =========================  ==================== 
 
 INVESTIGATOR-INITIATED STUDIES 
========================================  =========================  ==================== 
First report of the safety/tolerability   Wenhua Li, Department      639P 
 and preliminary antitumor activity        of Gastrointestinal        Poster presentation 
 of fruquintinib plus capecitabine         Medical Oncology,          (Colorectal cancer) 
 versus capecitabine as maintenance        Fudan University           Sunday, October 
 treatment for metastatic colorectal       Shanghai Cancer Center,    22, 2023 
 cancer: an open-label, randomized         Shanghai, China 
 phase Ib/II study 
========================================  =========================  ==================== 
Updated results from the multicenter      Fuxiang Zhou, Department   612P 
 phase II study of fruquintinib            of Radiation and           Poster presentation 
 plus mFOLFOX6/FOLFIRI as first-line       Medical Oncology,          (Colorectal cancer) 
 therapy in advanced metastatic            Zhongnan Hospital          Sunday, October 
 colorectal cancer (mCRC)                  of Wuhan University,       22, 2023 
                                           Wuhan, China 
========================================  =========================  ==================== 
A phase II study to evaluate the          Lu Wang, Liver surgery     637P 
 efficacy and safety of fruquintinib       department, Fudan          Poster presentation 
 combined with tislelizumab and            University Shanghai        (Colorectal cancer) 
 Hepatic artery infusion chemotherapy      Cancer Center, Shanghai,   Sunday, October 
 (HAIC) for advanced colorectal            China                      22, 2023 
 cancer liver metastases (CRLM) 
========================================  =========================  ==================== 
Fruquintinib combined with sintilimab     Pei Ma, Department         1494P 
 and chemotherapy as the first-line        of Oncology, The           Poster presentation 
 treatment in advanced naive EGFR-         First Affiliated           (NSCLC, metastatic) 
 and ALK-negative non-squamous non-small   Hospital of Nanjing        Monday, October 
 cell lung cancer (nsq-NSCLC): Updated     Medical University,        23, 2023 
 results of a phase II trial               Nanjing, Jiangsu, 
                                           China 
========================================  =========================  ==================== 
 

About Fruquintinib

Fruquintinib is a selective oral inhibitor of VEGFR -1, -2 and -3. VEGFR inhibitors play a pivotal role in inhibiting tumor angiogenesis. Fruquintinib was designed to have enhanced selectivity that limits off-target kinase activity, allowing for high drug exposure, sustained target inhibition, and flexibility for the potential use as part of combination therapy. Fruquintinib has been shown to be generally well tolerated in patients to date and is being investigated in combinations with other anti-cancer therapies.

Fruquintinib was approved for marketing by the China National Medical Products Administration (NMPA) in September 2018 and commercially launched in China in November 2018 under the brand name ELUNATE(R) . A marketing submission to the U.S. Food and Drug Administration ("FDA") was granted Priority Review and assigned a Prescription Drug User Fee Act (PDUFA) goal date of November 30, 2023. In addition, a submission to the European Medicines Agency ("EMA") was validated and accepted for review in June 2023, and a submission to the Japan Pharmaceuticals and Medical Devices Agency ("PMDA") took place in September 2023.

Takeda has the exclusive worldwide license to further develop, and commercialize, and manufacture fruquintinib outside of China. Fruquintinib is developed and marketed in China by HUTCHMED, in partnership with Eli Lilly and Company.

About HUTCHMED

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. It has approximately 5,000 personnel across all its companies, at the center of which is a team of about 1,800 in oncology/immunology. Since inception it has focused on bringing cancer drug candidates from in-house discovery to patients around the world, with its first three oncology drugs now approved and marketed in China. For more information, please visit: www.hutch-med.com or follow us on LinkedIn .

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the "safe harbor" provisions of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements reflect HUTCHMED's current expectations regarding future events, including but not limited to its expectations regarding the approval of a New Drug Application ("NDA") for fruquintinib for the treatment of CRC with the FDA, EMA and the PMDA and the timing of such approvals, the therapeutic potential of fruquintinib, the further clinical development for fruquintinib, its expectations as to whether any studies on fruquintinib would meet their primary or secondary endpoints, and its expectations as to the timing of the completion and the release of results from such studies. Forward-looking statements involve risks and uncertainties. Such risks and uncertainties include, among other things, assumptions regarding the timing and outcome of clinical studies and the sufficiency of clinical data to support NDA approval of fruquintinib for the treatment of patients with CRC or other indications in jurisdictions such as China, the U.S., the E.U. or Japan, its potential to gain approvals from regulatory authorities on an expedited basis or at all; the efficacy and safety profile of fruquintinib;, assumptions regarding enrollment rates and the timing and availability of subjects meeting a study's inclusion and exclusion criteria; changes to clinical protocols or regulatory requirements; unexpected adverse events or safety issues; the ability of fruquintinib, including as a combination therapy, to meet the primary or secondary endpoint of a study, to obtain regulatory approval in different jurisdictions and to gain commercial acceptance after obtaining regulatory approval; the potential market of fruquintinib for a targeted indication; the sufficiency of funding; and the impact of COVID-19 or other infectious diseases on general economic, regulatory and political conditions. In addition, as certain studies rely on the use of capecitabine, mFOLFOX6/FOLFIRI, tislelizumab or sintilimab as combination therapeutics, such risks and uncertainties include assumptions regarding their safety, efficacy, supply and continued regulatory approval. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. For further discussion of these and other risks, see HUTCHMED's filings with the U.S. Securities and Exchange Commission, The Stock Exchange of Hong Kong Limited and on AIM. HUTCHMED undertakes no obligation to update or revise the information contained in this press release, whether as a result of new information, future events or circumstances or otherwise.

Medical Information

This press release contains information about products that may not be available in all countries, or may be available under different trademarks, for different indications, in different dosages, or in different strengths. Nothing contained herein should be considered a solicitation, promotion or advertisement for any prescription drugs including the ones under development.

CONTACTS

 
Investor Enquiries                                           [phone] / [phone] / [e-mail] 
 
Media Enquiries 
  Ben Atwell / Alex Shaw, FTI Consulting                     [phone] / [phone] (Mobile) / +44 7779 
                                                             545 055 (Mobile) / [e-mail] 
  Zhou Yi, Brunswick                                         [phone] (Mobile) / [e-mail] 
 
Nominated Advisor 
  Atholl Tweedie / Freddy Crossley / Daphne Zhang, Panmure 
   Gordon                                                    [phone] 
 

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October 16, 2023 04:30 ET (08:30 GMT)