
- CSTONE receives advance payments, regulatory and commercial milestone payments as well as book revenue from Steinkares through the delivery of Sugemalimab to 10 Latin American (Latam) countries.
- This is the third large global commercialization partnership from CSTONE for SugemalimabWith additional offers in
Western Europe ,,Southeast Asia ,,Canada And other regions will soon be expected. CSTONE has received market approval for Sugemalimab in the EU and the EEA countries (Iceland ,,Liechtenstein AndNorway ) and theUnited Kingdom while at the same time the registration applications for additional indications are actively promoted.
As part of this cooperation, Steincares will be responsible for the regulatory matters and marketing activities of Sugemalimab in these regions. CSTONE will deliver Sugemalimab and receives advance payments, official and commercial milestone payments as well as income from product delivery.
Dr.
We also actively discuss with international partners in
About Sugemalimab
The monoclonal anti-PD-L1 antibody Sugemalimab was developed by CSTONE using the transgenic animal platform Omnirat®, which enables the production of completely human antibodies in one step. Sugemalimab is a completely human monoclonal anti-PD-L1 immunoglobulin G4 (IGG4) antibody full of length that can reduce the risk of immunogenicity and toxicity for patients-a unique advantage over similar drugs. The differentiated molecular design of Sugemalimab enables a double mechanism of action that not only blocks PD-1/PD-L1 interaction, but also induces antibody-dependent cellular phagocytosis (ADCP) by pd-l1-expressioned tumor cells with tumor-associated macrophages (tams) be networked. without damage to Effector T cells. This differentiation has led to competing effectiveness/security with a variety of tumor species.
The national Medical (TASE 🙂 Product management (NMPA) of
- In combination with chemotherapy as a first-line treatment of patients with metastatic squamous epithelial carcinoma and non-record-epithelial carcinoma NSCLC;
- For treating patients with inoperable NSCLC in stage III, whose illness has not advanced after simultaneous or sequential platinum -based radiochemotherapy;
- To treat patients with recurrent or refractory extranodal nk/t cell lymphoma;
- In combination with fluorouracil and platinum -based chemotherapy as an initial treatment of patients with inoperable, locally advanced, recurrent or metastatic ESCC; And
- In combination with fluoropyrimidine and platinum-containing chemotherapy as an initial treatment for inoperable, locally advanced or metastatic adenocarcinoma of the gastrointestinal or gastroesophageal transition (g/G/GEJ) with a PD-L1 expression (combined positive score (CPS) ¥ 5) .
The European Commission (EC) has approved Sugemalimab (brand name: CEJEMLY ®) in combination with a platinum-based chemotherapy for the first-line treatment of patients with metastatic NSCLC without sensitizing EGFR mutations or genomic tumorabrations of ALK, ROS1 or RET.
The regulatory authority for medicines and health products (MHRA) in the
About Cstone
CSTONE (HKEX: 2616) was founded at the end of 2015 and is an innovation -driven biopharmaceutical company that focuses on the research and development of cancer therapies. We devote ourselves to the solution of uncovered medical needs of patients
Ir-contact: ir@cstonepharma.com
PR contact: pr@cstonepharma.com
About Steincares
Steinkares is a leader in the commercialization and distribution of special products for health care
For more information, see http://www.steincares.com/ or follow the company LinkedIn.
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