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CS1001+ Fluorouracil+Cisplatin

CStone Pharmaceuticals · Phase 3 active Small molecule

CS1001 is a PD-L1 inhibitor that blocks immune checkpoint signaling, combined with fluorouracil and cisplatin chemotherapy to enhance anti-tumor immunity and direct cytotoxic effects.

CS1001 is a PD-L1 inhibitor that blocks immune checkpoint signaling, combined with fluorouracil and cisplatin chemotherapy to enhance anti-tumor immunity and direct cytotoxic effects. Used for Gastric or gastroesophageal junction cancer, Esophageal squamous cell carcinoma.

At a glance

Generic nameCS1001+ Fluorouracil+Cisplatin
SponsorCStone Pharmaceuticals
Drug classPD-L1 inhibitor + chemotherapy combination
TargetPD-L1
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

CS1001 (an anti-PD-L1 monoclonal antibody) restores T-cell-mediated anti-tumor immunity by blocking the PD-L1/PD-1 interaction. When combined with fluorouracil (a pyrimidine antimetabolite) and cisplatin (a platinum-based alkylating agent), the chemotherapy agents provide direct cytotoxic effects while potentially enhancing immunogenicity, creating a synergistic triple-modality approach for solid tumors.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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