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Study on the efficacy and safety of recombinant human endostatin combined with PD1 inhibitor and chemotherapy in the treatment of pancreatic cancer

Study on the efficacy and safety of recombinant human endostatin combined with PD1 inhibitor and chemotherapy in the treatment of pancreatic cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064322
Enrollment
Unknown
Registered
2022-10-02
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic cancer

Interventions

experimental group:Endostar + Camrelizumab + Chemotherapy
control group:Chemotherapy

Sponsors

The Affiliated People's Hospital of Jiangsu University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Pancreatic cancer was confirmed by pancreatic puncture, lymph node biopsy, or exfoliative cytology of peritoneal effusion, or diagnosed by imaging examination combined with laboratory examination and clinical symptom; 2. Patients with pancreatic cancer are diagnosed by surgical and pathological sections and whose recurrence and metastasis cannot be resected after radical resection; 3. All patients were proved to have at least one objectively measurable or evaluable tumor focus by imaging examination; 4. Age >= 18 years old, gender and pathological types are not limited, Karnofsky Performance Status (KPS) >= 60 points before chemotherapy, expect to receive at least two cycles of chemotherapy, estimated survival time > 3 months; 5. Blood routine, liver function, renal function, heart function, and lung function are basically normal; 6. Progesterone, adrenocortical hormone, and metabolic hormone were not treated within 3 weeks before chemotherapy; 7. No primary malignant tumors are other than the pancreas; 8. Signed informed consent and able to cooperate with treatment, willing to long-term follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with rapid progression within two cycles of chemotherapy; 2. Patients who have severe toxic reactions during chemotherapy and cannot tolerate continued chemotherapy; 3. Patients who are pregnant or lactating; 4. Patients with other primary tumors or poor compliance; 5. Diabetes or infection is not effectively controlled or other serious non-tumor factors hinder further chemotherapy; 6. Patients who want to withdraw for a variety of reasons.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Progression free survival;Overall survival;Tumor marker;Safety;

Countries

China

Contacts

Public ContactYu Fan

The Affiliated People's Hospital of Jiangsu University

yuf36@sina.com+86 13952862305

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026