[
  {
    "Asset": "Zolbetuximab / VYLOY",
    "Company / rights context": "Astellas",
    "Modality": "Antibody",
    "Map stage": "Approved",
    "Reviewed status": "FDA approved; first-line HER2-negative, CLDN18.2-positive advanced gastric/GEJ cancer with chemotherapy",
    "Competitive relevance / caveat": "Commercial reference; Phase 3 program adding pembrolizumab.",
    "Gosset drug_id": "67f6aa6a3623f1d2313f6347",
    "Gosset name": "zolbetuximab",
    "Gosset phase": "Approved",
    "Gosset maintenance status": "Approved",
    "Trial identifiers": "NCT03504397; NCT03653507; NCT06901531",
    "Registry status by trial": "NCT03504397: ACTIVE_NOT_RECRUITING; NCT03653507: ACTIVE_NOT_RECRUITING; NCT06901531: RECRUITING",
    "Primary evidence": "https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-zolbetuximab-clzb-chemotherapy-gastric-or-gastroesophageal-junction-adenocarcinoma",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT03504397; https://clinicaltrials.gov/study/NCT03653507; https://clinicaltrials.gov/study/NCT06901531"
  },
  {
    "Asset": "Satri-cel / CT041",
    "Company / rights context": "CARsgen",
    "Modality": "Cell therapy",
    "Map stage": "Approved",
    "Reviewed status": "China approved 22 Jun 2026; HER2-negative, CLDN18.2-positive advanced gastric/GEJ cancer after at least two prior lines",
    "Competitive relevance / caveat": "Regional approval overrides raw Phase 2 classification; pancreatic adjuvant expansion remains investigational.",
    "Gosset drug_id": "68cc48c7d1b9e2725213eaa7",
    "Gosset name": "satricabtagene autoleucel",
    "Gosset phase": "2",
    "Gosset maintenance status": "Active",
    "Trial identifiers": "NCT04581473; NCT05911217",
    "Registry status by trial": "NCT04581473: ACTIVE_NOT_RECRUITING; NCT05911217: RECRUITING",
    "Primary evidence": "https://www1.hkexnews.hk/listedco/listconews/sehk/2026/0622/2026062200474.pdf",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT04581473; https://clinicaltrials.gov/study/NCT05911217"
  },
  {
    "Asset": "IBI343 / TAK-921 (arcotatug tavatecan)",
    "Company / rights context": "Innovent; Takeda outside Greater China",
    "Modality": "ADC",
    "Map stage": "Filing / readout",
    "Reviewed status": "China NDA accepted; positive Phase 3 interim analysis announced 4 Jun 2026",
    "Competitive relevance / caveat": "TOP1-payload ADC; later-line gastric filing and Phase 3 pancreatic expansion. Full comparative data remain important.",
    "Gosset drug_id": "6833c83f67141c9b36be4c51",
    "Gosset name": "arcotatug tavatecan",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT06238843; NCT07066098",
    "Registry status by trial": "NCT06238843: ACTIVE_NOT_RECRUITING; NCT07066098: RECRUITING",
    "Primary evidence": "https://en.innoventbio.com/InvestorsAndMedia/PressReleaseDetail?key=601; https://www.takeda.com/newsroom/newsreleases/2025/innovent/",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT06238843; https://clinicaltrials.gov/study/NCT07066098"
  },
  {
    "Asset": "LM-302 (tecotabart vedotin; TPX-4589)",
    "Company / rights context": "LaNova / Sino Biopharmaceutical",
    "Modality": "ADC",
    "Map stage": "Filing / readout",
    "Reviewed status": "China NDA accepted; positive pivotal interim analysis announced 23 Jun 2026",
    "Competitive relevance / caveat": "MMAE ADC; both pivotal endpoints reported met; detailed results planned early 2027. Current sponsor replaces historical BMS attribution.",
    "Gosset drug_id": "68cd525180f6166b24a8eece",
    "Gosset name": "tpx-4589",
    "Gosset phase": "3",
    "Gosset maintenance status": "Active",
    "Trial identifiers": "NCT06351020; NCT07385703",
    "Registry status by trial": "NCT06351020: ACTIVE_NOT_RECRUITING; NCT07385703: RECRUITING",
    "Primary evidence": "https://www1.hkexnews.hk/listedco/listconews/sehk/2026/0623/2026062300456.pdf",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT06351020; https://clinicaltrials.gov/study/NCT07385703"
  },
  {
    "Asset": "Sonesitatug vedotin / AZD0901 / CMG901",
    "Company / rights context": "AstraZeneca",
    "Modality": "ADC",
    "Map stage": "Filing / readout",
    "Reviewed status": "Phase 3 positive OS topline; no approval established in reviewed sources",
    "Competitive relevance / caveat": "MMAE ADC; 3L+ OS primary and 2L+ OS secondary endpoints met; 2L+ PFS primary not significant. First-line Phase 3 also recruiting.",
    "Gosset drug_id": "68cbf5a53b71859dcd59d7c9",
    "Gosset name": "sonesitatug vedotin",
    "Gosset phase": "3",
    "Gosset maintenance status": "Active",
    "Trial identifiers": "NCT06346392; NCT07431281",
    "Registry status by trial": "NCT06346392: ACTIVE_NOT_RECRUITING; NCT07431281: RECRUITING",
    "Primary evidence": "https://www.astrazeneca.com/media-centre/press-releases/2026/sone-ve-improved-survival-in-gastric-cancers.html",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT06346392; https://clinicaltrials.gov/study/NCT07431281"
  },
  {
    "Asset": "SHR-A1904 (garetatug rezetecan)",
    "Company / rights context": "Hengrui",
    "Modality": "ADC",
    "Map stage": "Phase 3 underway",
    "Reviewed status": "Phase 3 recruiting",
    "Competitive relevance / caveat": "TOP1 ADC; second-line gastric/GEJ trial versus chemotherapy; China sites in registry.",
    "Gosset drug_id": "693f5636d91942c1924b6507",
    "Gosset name": "garetatug rezetecan",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT06649292",
    "Registry status by trial": "NCT06649292: RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT06649292"
  },
  {
    "Asset": "JS107",
    "Company / rights context": "Junshi",
    "Modality": "ADC",
    "Map stage": "Phase 3 underway",
    "Reviewed status": "Two Phase 3 trials recruiting",
    "Competitive relevance / caveat": "MMAE ADC; later-line monotherapy and first-line toripalimab/chemotherapy regimens.",
    "Gosset drug_id": "682e5859a83c5cea4839612d",
    "Gosset name": "JS107",
    "Gosset phase": "3",
    "Gosset maintenance status": "Active",
    "Trial identifiers": "NCT07284134; NCT07584135",
    "Registry status by trial": "NCT07284134: RECRUITING; NCT07584135: RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT07284134; https://clinicaltrials.gov/study/NCT07584135"
  },
  {
    "Asset": "BL-M05D1",
    "Company / rights context": "Sichuan Baili / SystImmune",
    "Modality": "ADC",
    "Map stage": "Phase 3 underway",
    "Reviewed status": "Phase 3 recruiting",
    "Competitive relevance / caveat": "Later-line gastric/GEJ ADC program; registry sponsor Sichuan Baili, Gosset lead SystImmune.",
    "Gosset drug_id": "67f7f9ed9060f7552a055202",
    "Gosset name": "BL-M05D1",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT07518147",
    "Registry status by trial": "NCT07518147: RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT07518147"
  },
  {
    "Asset": "ASKB589",
    "Company / rights context": "AskGene",
    "Modality": "Antibody",
    "Map stage": "Phase 3 underway",
    "Reviewed status": "Phase 3 active, not recruiting",
    "Competitive relevance / caveat": "First-line CAPOX plus PD-1 inhibitor combination; estimated primary completion Dec 2026.",
    "Gosset drug_id": "67f804f94afab6023b2a958a",
    "Gosset name": "ASKB589",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT06206733",
    "Registry status by trial": "NCT06206733: ACTIVE_NOT_RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT06206733"
  },
  {
    "Asset": "FG-M108 / M108",
    "Company / rights context": "FutureGen (registry sponsor)",
    "Modality": "Antibody",
    "Map stage": "Phase 3 underway",
    "Reviewed status": "Gastric Phase 3 recruiting; pancreatic Phase 3 not yet recruiting",
    "Competitive relevance / caveat": "Gastric trial selects HER2-negative, PD-L1 CPS<5 disease and compares M108 plus CAPOX with placebo plus CAPOX. Gastric registry last updated Feb 2024.",
    "Gosset drug_id": "67f9266da8a467cb7b3fcc63",
    "Gosset name": "M108",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT06177041; NCT07383922",
    "Registry status by trial": "NCT06177041: RECRUITING; NCT07383922: NOT_YET_RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT06177041; https://clinicaltrials.gov/study/NCT07383922"
  },
  {
    "Asset": "ASP2138",
    "Company / rights context": "Astellas",
    "Modality": "Bispecific",
    "Map stage": "Phase 3 underway",
    "Reviewed status": "Phase 3 recruiting; first patient dosed Aug 2026",
    "Competitive relevance / caveat": "CLDN18.2 x CD3; subcutaneous administration; first-line pembrolizumab/chemotherapy combination.",
    "Gosset drug_id": "67f90166f079deded49212ad",
    "Gosset name": "ASP2138",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT07673887",
    "Registry status by trial": "NCT07673887: RECRUITING",
    "Primary evidence": "https://newsroom.astellas.com/2026-08-25-astellas-doses-first-patient-in-phase-3-study-of-asp2138-in-cldn18-2-postive-and-her2-negative-locally-advanced-unresectable-or-metastatic-gastric-or-gastroesophageal-junction-gej-adenocarcinoma",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT07673887"
  },
  {
    "Asset": "QLS31905",
    "Company / rights context": "Qilu",
    "Modality": "Bispecific",
    "Map stage": "Phase 3 underway",
    "Reviewed status": "Pancreatic Phase 3 recruiting; gastric Phase 3 not yet recruiting",
    "Competitive relevance / caveat": "CLDN18.2 x CD3; two first-line indication strategies. Do not label the gastric Phase 3 as recruiting.",
    "Gosset drug_id": "67f7ea269060f7552a054a0a",
    "Gosset name": "QLS-31905",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT07079228; NCT07716449",
    "Registry status by trial": "NCT07079228: RECRUITING; NCT07716449: NOT_YET_RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT07079228; https://clinicaltrials.gov/study/NCT07716449"
  },
  {
    "Asset": "Osemitamab / TST001",
    "Company / rights context": "Transcenta",
    "Modality": "Antibody",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Phase 3 registered, not yet recruiting; clinical evidence from earlier phases",
    "Competitive relevance / caveat": "Enhanced-effector antibody; planned first-line pembrolizumab/chemotherapy study. Registration is not evidence that Phase 3 dosing began.",
    "Gosset drug_id": "68cc48d0d1b9e2725213eaaa",
    "Gosset name": "osemitamab",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT06093425",
    "Registry status by trial": "NCT06093425: NOT_YET_RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT06093425"
  },
  {
    "Asset": "ATG-022",
    "Company / rights context": "Antengene",
    "Modality": "ADC",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Phase 3 registered, not yet recruiting",
    "Competitive relevance / caveat": "MMAE ADC; Phase 3 listing updated 31 Aug 2026. Clinical Phase 1/2 program exists.",
    "Gosset drug_id": "67f820d94afab6023b2ab30a",
    "Gosset name": "ATG-022",
    "Gosset phase": "3",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT07795346",
    "Registry status by trial": "NCT07795346: NOT_YET_RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT07795346"
  },
  {
    "Asset": "Givastomig / ABL111",
    "Company / rights context": "NovaBridge / ABL Bio",
    "Modality": "Bispecific",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Randomized Phase 2 recruiting; Phase 3 planned, not established as started",
    "Competitive relevance / caveat": "CLDN18.2 x 4-1BB; first-line immunochemotherapy; low-expression eligibility. Sponsor aims for Phase 3 as early as year-end 2026.",
    "Gosset drug_id": "67f9251aa8a467cb7b3fcb15",
    "Gosset name": "givastomig",
    "Gosset phase": "2",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT07432295; NCT04900818",
    "Registry status by trial": "NCT07432295: RECRUITING; NCT04900818: RECRUITING",
    "Primary evidence": "https://www.novabridge.com/news-releases/news-release-details/novabridge-reports-first-half-2026-financial-results-and",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT07432295; https://clinicaltrials.gov/study/NCT04900818"
  },
  {
    "Asset": "ASP546C / XNW27011",
    "Company / rights context": "Astellas / Evopoint",
    "Modality": "ADC",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Phase 1/2 recruiting",
    "Competitive relevance / caveat": "TOP1 ADC; ex-Greater-China rights licensed to Astellas.",
    "Gosset drug_id": "69c34068774377403427d952",
    "Gosset name": "ASP546C",
    "Gosset phase": "2",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT07488676; NCT06792435",
    "Registry status by trial": "NCT07488676: RECRUITING; NCT06792435: ACTIVE_NOT_RECRUITING",
    "Primary evidence": "https://www.astellas.com/system/files/news/2025-05/ee939af947/20250530_en_1.pdf",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT07488676; https://clinicaltrials.gov/study/NCT06792435"
  },
  {
    "Asset": "RC118",
    "Company / rights context": "RemeGen",
    "Modality": "ADC",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Phase 1/2 recruiting in registry; updates dated Jan 2025",
    "Competitive relevance / caveat": "MMAE ADC; earlier clinical watchlist, with aged registry timelines.",
    "Gosset drug_id": "67f8159f4afab6023b2aa681",
    "Gosset name": "RC118",
    "Gosset phase": "2",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT05205850; NCT06038396",
    "Registry status by trial": "NCT05205850: RECRUITING; NCT06038396: RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT05205850; https://clinicaltrials.gov/study/NCT06038396"
  },
  {
    "Asset": "SKB315 / MK-1200 (Gosset: lucansatuzumab)",
    "Company / rights context": "Kelun; historical Merck trial sponsor",
    "Modality": "ADC",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Kelun Phase 1 recruiting; Phase 2 registered, not yet recruiting; Merck Phase 1/2 completed",
    "Competitive relevance / caveat": "TOP1 ADC. Ownership/rights not inferred from a completed Merck trial; distinct regional trial statuses retained.",
    "Gosset drug_id": "69e773a484eb800a45182476",
    "Gosset name": "lucansatuzumab",
    "Gosset phase": "2",
    "Gosset maintenance status": "Active",
    "Trial identifiers": "NCT05367635; NCT06242691; NCT07609667",
    "Registry status by trial": "NCT05367635: RECRUITING; NCT06242691: COMPLETED; NCT07609667: NOT_YET_RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT05367635; https://clinicaltrials.gov/study/NCT06242691; https://clinicaltrials.gov/study/NCT07609667"
  },
  {
    "Asset": "Spevatamig / PT886",
    "Company / rights context": "Phanes",
    "Modality": "Bispecific",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Phase 1/2 recruiting",
    "Competitive relevance / caveat": "CLDN18.2 x CD47; differentiates through macrophage checkpoint biology.",
    "Gosset drug_id": "680390dde845f2ae11fe14d6",
    "Gosset name": "spevatamig",
    "Gosset phase": "2",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT05482893",
    "Registry status by trial": "NCT05482893: RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT05482893"
  },
  {
    "Asset": "TAC01-CLDN18.2",
    "Company / rights context": "Triumvira",
    "Modality": "Cell therapy",
    "Map stage": "Earlier / pending",
    "Reviewed status": "Phase 1/2 active, not recruiting; last update Feb 2025",
    "Competitive relevance / caveat": "T-cell antigen coupler (TAC) product. Kept distinct from conventional CAR-T despite broad Gosset classification.",
    "Gosset drug_id": "67f814374afab6023b2aa4d4",
    "Gosset name": "TAC01-CLDN18.2",
    "Gosset phase": "2",
    "Gosset maintenance status": "Stale",
    "Trial identifiers": "NCT05862324",
    "Registry status by trial": "NCT05862324: ACTIVE_NOT_RECRUITING",
    "Primary evidence": "",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT05862324"
  },
  {
    "Asset": "SOT102",
    "Company / rights context": "SOTIO",
    "Modality": "ADC",
    "Map stage": "Discontinued",
    "Reviewed status": "Clinical development discontinued; trial terminated",
    "Competitive relevance / caveat": "Overrides Gosset Active label; sponsor-authored paper reports unexpected toxicities and discontinued development.",
    "Gosset drug_id": "67f907faf079deded4921972",
    "Gosset name": "SOT102",
    "Gosset phase": "2",
    "Gosset maintenance status": "Active",
    "Trial identifiers": "NCT05525286",
    "Registry status by trial": "NCT05525286: TERMINATED",
    "Primary evidence": "https://link.springer.com/article/10.1186/s12885-026-16185-x",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT05525286"
  },
  {
    "Asset": "EO-3021 / SYSA1801",
    "Company / rights context": "Elevation / CSPC (territory-specific history)",
    "Modality": "ADC",
    "Map stage": "Discontinued",
    "Reviewed status": "Elevation program discontinued; global territory status not established",
    "Competitive relevance / caveat": "Elevation discontinuation must not automatically be generalized to all CSPC territories. Chinese Phase 1 registry remains Unknown and old.",
    "Gosset drug_id": "67f91cb8a8a467cb7b3fc377",
    "Gosset name": "SYSA1801",
    "Gosset phase": "Discontinued",
    "Gosset maintenance status": "Discontinued",
    "Trial identifiers": "NCT05980416; NCT05009966",
    "Registry status by trial": "NCT05980416: TERMINATED; NCT05009966: UNKNOWN",
    "Primary evidence": "https://www.prnewswire.com/news-releases/elevation-oncology-to-discontinue-development-of-eo-3021-advancing-eo-1022-while-evaluating-strategic-options-302406229.html",
    "Trial URLs": "https://clinicaltrials.gov/study/NCT05980416; https://clinicaltrials.gov/study/NCT05009966"
  }
]
