OncoMatch/Clinical Trials/NCT06491472
Ivonescimab(AK112/SMT112) in Combination With Stereotactic Body Radiation Therapy and Chemotherapy in Patients With Pancreatic Cancer
Is NCT06491472 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Ivonescimab and Gemcitabine for pancreatic cancer.
Treatment: Ivonescimab · Gemcitabine · Nab paclitaxel — This study is an open-label, single-arm Phase II clinical study to evaluate the efficacy and safety of ivonescimab(AK112/SMT112) in combination with stereotactic body radiation therapy and chemotherapy in patients with pancreatic cancer
Check if I qualifyExtracted eligibility criteria
Cancer type
Pancreatic Cancer
Biomarker criteria
Excluded: BRCA1 germline mutation
Excluded: BRCA2 germline mutation
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Cannot have received: radiotherapy
Exception: no overlap between the secondary radiotherapy site and the original radiotherapy site
No previous history of radiotherapy or no overlap between the secondary radiotherapy site and the original radiotherapy site
Cannot have received: agent targeting T cell costimulation or immune checkpoint pathways (anti-PD 1, anti-PD L1, anti-PD L2, anti-CTLA 4, anti-CD137, anti-OX40 antibody)
Prior exposure to any agent targeting T cell costimulation or immune checkpoint pathways (e.g., anti-PD 1, anti-PD L1, anti-PD L2, anti-CTLA 4, anti CD137 or anti-OX40 antibody, etc)
Cannot have received: chemotherapy
Received chemotherapy...within 28 days before the study
Cannot have received: tyrosine kinase inhibitor
Received...tyrosine kinase inhibitors...within 28 days before the study
Cannot have received: immunotherapy (interleukin, interferon, thymosin)
Received...immunotherapy (such as interleukin, interferon or thymosin)...within 28 days before the study
Cannot have received: other anti-tumor therapy
Received...other anti-tumor therapy within 28 days before the study
Cannot have received: Chinese medicine with anti-tumor indications
received Chinese medicine with anti-tumor indications within 14 days before the administration
Cannot have received: major surgery
Has undergone major surgery within 30 days prior to the first dose of study treatment
Cannot have received: radical radiotherapy
Exception: Palliative radiotherapy was allowed 2 weeks before administration, and the radiotherapy dose was in line with local palliative treatment standards
Has received radical radiotherapy within 3 months before the study; Palliative radiotherapy was allowed 2 weeks before administration, and the radiotherapy dose was in line with local palliative treatment standards
Lab requirements
Blood counts
Kidney function
Liver function
Has adequate organ function
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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