drugset / Trial / NCT07208539

AG Followed by FOLFIRINOX Both Combined With PD-L1 Antibodies as a Conversion Therapy for Borderline Resectable and Locally Advanced Pancreatic Cancer.

NCT07208539

Phase 2 Not yet recruiting 77 enrolled Shanghai Zhongshan Hospital
NaParallel-groupOpen-labelTreatment

Summary

The goal of this interventional study is to learn about the clinical efficacy of sequential therapy (albumin paclitaxel, gemcitabine combined with PD-L1 antibodies, followed by liposomal irinotecan, oxaliplatin and 5-FU/LV combined with PD-L1 antibodies). The main questions it aims to answer are: Does the sequential therapy increase the resection rate of borderline resectable / locally advanced pancreatic cancer? Does the sequential therapy represent an effective and safe treatment? Participants will receive two distinct chemotherapy regimens, each combined with a PD-L1 antibody, administered in sequence for two cycles each.

Timeline

Start
2025-10-10
Primary completion
2026-04-09
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody
Subject Gemcitabine Small molecule
Subject Irinotecan Small molecule
Subject Oxaliplatin Small molecule
Subject Paclitaxel Small molecule
Subject Treatment: AG & anti-PD-L1 + FOLFIRINOX & anti-PD-L1 Unknown
Subject fluorouracil Small molecule