Sugemalimab is under clinical development by CStone Pharmaceuticals and currently in Phase I for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma). According to GlobalData, Phase I drugs for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma) have a 72% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Sugemalimab’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Sugemalimab overview
Sugemalimab (Cejemly) is an recombinant human anti-PD-L1 monoclonal antibody. It is formulated as solution for intravenous route of administration. Cejemly in combination with pemetrexed and carboplatin is indicated as first-line treatment of patients with metastatic nonsquamous NSCLC, with no EGFR or ALK genomic tumor aberrations and in combination with paclitaxel and carboplatin as first-line treatment of patients with metastatic squamous NSCLC. Cejemly is indicated for the treatment of patients with unresectable stage III non-small cell lung cancer (NSCLC) whose disease has not progressed following concurrent or sequential platinum-based chemoradiotherapy. It is being developed based on OmniRat transgenic animal platform.
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Sugemalimab (Cejemly) is under development for the treatment of solid tumors including endometrial cancer, cholangiocarcinoma, recurrent head and neck squamous cell carcinoma (HNSCC).
CStone Pharmaceuticals overview
CStone Pharmaceuticals is a biopharmaceutical company. It develops and commercializes immuno-oncology and precision medicine to address the unmet medical needs of cancer patients. The company’s pipeline product portfolio includes Ivosidenib (CS3010) for the treatment of acute myeloid leukemia (AML); CS1001 to treat solid tumors; Avapritinib (CS3007) for the treatment of liver diseases; CS1002, CS1003, CS3006, CS3003, CS3002 to treat solid tumors. CStone Pharmaceuticals operates clinical research institutions for developing anti-cancer drugs. The company’s partners include Agios Inc, Blueprint Medicines Corp and WuXi Biologics. CStone Pharmaceuticals is headquartered in Shanghai, China.
For a complete picture of Sugemalimab’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
