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CTTQ-Akeso

CTTQ-Akeso (Shanghai) Biomed. Tech. Co., Ltd. (CTTQ-Akeso), with registered capital of RMB 690 million, is an innovative biomedical company jointly established by Akeso, Inc. (9926.HK) and Chia Tai Tianqing Pharmaceutical Group Co., Ltd... CTTQ-Akeso focuses on the R&D of innovative biologics, industrialization of research results, technology transfer and commission processing, and is committed to the R&D and commercialization of the anti PD-1 monoclonal antibody drug Penpulimab monoclonal antibody injection (安尼可®) for tumor immunotherapy.

安尼可® (Penpulimab injection)

At present, 安尼可® is the only PD-1 monoclonal antibody that applies the immunoglobulin G1 (‘‘IgG1’’) subtype modified by the fragment crystallizable (Fc) segment in the world, which has a lower antigen binding off-rate and a unique binding epitope as demonstrated by analysis on crystal structure. These features allow 安尼可® to effectively and continuously block PD-1/PD-L1 binding, thus differentiating it from PD-1 products on the market, and may enable安尼可® to more effectively enhance immunotherapeutic efficacy and reduce immune-related adverse reactions. The main indications for安尼可® include lung cancer, liver cancer, gastric cancer, nasopharyngeal cancer, esophageal cancer, classical Hodgkin’s lymphoma, mesothelioma, thymic cancer, urothelial cancer, bile duct cancer and neuroendocrine cancer. Currently,  phase III clinical studies on 安尼可® plus Anlotinib in the first-line treatment of non-phosphorous non-small cell lung cancer, liver cancer and gastric cancer, have all entered the final stage.

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Milestones for安尼可®

01
2023
Marketing approval: In January 2023, Penpulimab was officially approved for first-line treatment of locally advanced or metastatic sq-NSCLC.
08
2021
Marketing approval: In August 2021, Penpulimab was officially approved for marketing by the National Medical Products Administration (NMPA) for the treatment of relapsed or refractoryclassical Hodgkin’s lymphoma (r/r cHL) after at least second-line systemic chemotherapy treatment.
08
2021
NDA:In August 2021, NDA of Penpulimab for third-line treatment of metastatic nasopharyngeal carcinoma was submitted and was accepted by the NMPA.
07
2021
NDA: In July 2021, the marketing application for Penpulimab plus chemotherapy in the first-line treatment of locally advanced or metastatic squamous non-small cell lung cancer was accepted by the NMPA.
05
2021
BLA: In May 2021, Akeso submitted a Biologics License Application (BLA) for Penpulimab to the Food and Drug Administration of the United States (FDA) for the third-line treatment of metastatic nasopharyngeal carcinoma.
Address

Fenglin Building, No.420 Fenglin Road, Xuhui District, Shanghai

Service Hotline

400-008-5183 (working days: 9:00–17:00)

Adverse Event Reporting

Click to provide us with more information

Note: If your report involves an adverse event of CTTQ-Akeso’s products, the relevant patient information and data will be disclosed to CTTQ-Akeso’s pharmacovigilance department in accordance with the applicable laws and regulations, and the relevant personnel may follow up with you on the adverse event. The information will be input into CTTQ-Akeso’s drug safety database and may be legally required to reported to relevant regulatory departments.

  • About Us
    • Corporate Profile
    • Management Team
    • Milestones
    • Awards
    • Our Vision
    • Affiliates
      • CTTQ Akesobio
      • Akeso Pharma
    • Contact Us
  • R&D and science
    • R&D Platform
    • Pipelines
    • Products Center
    • Manufacturing
    • Subject Recruitment
    • Expanded Access Policy
  • Collaborations
  • Investor Relations
    • Listing Documents
    • Financial Reports
    • Presentations
    • IR Monthly Reports
    • Announcements and Circulars
    • Corporate Governance
    • IR Calendar
    • IR Contact
  • Media
  • Career
    • Now Hiring
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