RecruitingPhase 2NCT06050317

Sintilimab Combined With Chemotherapy and Radiotherapy in Patients With Inoperable Pancreatic Cancer

Sintilimab Plus Chemotherapy and Radiotherapy for Patients With Inoperable Pancreatic Cancer: a Single-arm, Exploratory, Phase II Trial


Sponsor

Shandong Cancer Hospital and Institute

Enrollment

25 participants

Start Date

Aug 18, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Hypothesis: Survival benefits could be found in Sintilimab plus chemotherapy and radiotherapy in patients with inoperable pancreatic cancer.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study tests combining an immunotherapy drug (sintilimab) with chemotherapy and radiation for patients with advanced pancreatic cancer that cannot be surgically removed. Researchers hope this combination can improve outcomes better than standard treatment alone. **You may be eligible if...** - You have been diagnosed with locally advanced pancreatic cancer that cannot be surgically removed, confirmed by tissue biopsy - You have not yet received any cancer treatment for this condition - You are in good overall health and have a life expectancy of more than 3 months - Your blood counts and organ function are within acceptable ranges **You may NOT be eligible if...** - You were diagnosed with another cancer in the past 3 years - You are currently in another clinical trial - You have active autoimmune conditions or are on immune-suppressing medications - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSintilimab Plus mFFN or NALIRIFOX and Radiation

Sintilimab Plus mFFN or NALIRIFOX and Radiation


Locations(1)

Department of Radiation Oncology, Shandong Cancer Hospital and Institute

Jinan, Shandong, China

View Full Details on ClinicalTrials.gov

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NCT06050317


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