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OncoMatch/Clinical Trials/NCT06791083

Clinical Study of Envafolimab Combined With Fruquintinib and Chemotherapy for Neoadjuvant Treatment of Gastric Cancer

Is NCT06791083 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Envafolimab and Fruquintinib for gastric cancer.

Phase 2RecruitingFirst Affiliated Hospital of Fujian Medical UniversityNCT06791083Data as of Jun 2026Location: China

Treatment: Envafolimab · FruquintinibTo observe and evaluate the neoadjuvant treatment of Envafolimab combined with Fruquintinib and chemotherapy for locally advanced gastric/gastroesophageal junction carcinoma

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Envafolimab

Targeted therapy

Fruquintinib

Cancer type

Gastric Cancer

Biomarker criteria

Excluded: HER2 (ERBB2) positive

Known HER2-positive patients

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: any systemic anti-tumor therapy

received other systemic anti-tumor therapy, including chemotherapy, signal transduction inhibitors, immunotherapy, and other investigational drugs within 4 weeks prior to enrollment

Cannot have received: investigational drug

Participated in other drug clinical trials and received at least one drug therapy within 4 weeks prior to enrollment

Lab requirements

Blood counts

Absolute neutrophil count ≥1.5×109/L; Platelet ≥80×109/L; Hemoglobin ≥90g/L

Kidney function

Serum creatinine (Cr) ≤1.5×ULN or creatinine clearance (CCr)≥60ml/min; endogenous creatinine clearance > 50ml/min

Liver function

Total bilirubin < 1.5 ULN; ALT and AST < 2.5 ULN (< 5 ULN in patients with liver metastasis)

Cardiac function

NYHA heart function Grade ≤ II and left ventricular ejection fraction (LVEF) ≥ 50%

Absolute neutrophil count ≥1.5×109/L; Platelet ≥80×109/L; Hemoglobin ≥90g/L; Total bilirubin < 1.5 ULN; ALT and AST < 2.5 ULN (< 5 ULN in patients with liver metastasis); Serum creatinine (Cr) ≤1.5×ULN or creatinine clearance (CCr)≥60ml/min; endogenous creatinine clearance > 50ml/min; NYHA heart function Grade > II or left ventricular ejection fraction (LVEF) < 50% [excluded]

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06791083 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Are patients with ERBB2 alterations eligible?

No. ERBB2 positive is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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