CNClinicalTrials.govClinical trialPhase 2Active, not recruiting
Perioperative Surufatinib Plus Sintilimab Combined With Chemotherapy in Gastric/Gastroesophageal Junction Adenocarcinoma
Official record
- Identifier
NCT06447636- Recruiting locations
country
China- Interventions studied
- SurufatinibSintilimabOxaliplatinS1
- Lead sponsor
- Fudan University
- Target enrolment
- 20 participants
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Status
- Active, not recruiting
- First posted
- Jun 7, 2024
- Last updated on the registry
- Jul 24, 2026
- Age
- 18 Years – 75 Years
- Sex
- ALL
- Study contact
- No public contact is listed on the official record.
- Eligibility criteria
Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.
Inclusion Criteria: * signed informed consent * patients age 18-75 years; * Histologically CT/MRI confirmed cT3-4bNanyM0 gastric or GEJ adenocarcinoma; * ECOG 0-1, no surgery contraindications; * Expected survival ≥3 months; Exclusion Criteria: * signs of distant metastases * Prior chemotherapy, radiotherapy, surgery for gastric cancer; * Significant cardiovascular disease * major surgical procedure within 4 weeks prior to initiation of study treatment * current treatment with anti-viral therapy or HBV * pregnancy or breastfeeding * history of malignancy within 5 years prior to screening * Present or history of any autoimmune disease or immune deficiency; * Prior therapy with a PD-1, anti-PD-Ligand 1 (PD-L1) or CTLA-4 agent; * There are active gastric and duodenal ulcers, ulcerative colitis and other gastrointestinal diseases, or active bleeding in unresectable tumors. * Poorly controlled hypertension or diabetes;
- Indexed under
- Gastric Cancer
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