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Clinical Trial Summary

To evaluate the efficacy of PD-L1/CTLA4 BsAb for the second line treatment and the combination with chemotherapy for the first line treatment in pancreatic cancer


Clinical Trial Description

Subjects who signed the informed consent were assigned to three cohorts according to the actual treatment status. Cohort 1 enrolled subjects receiving PD-L1/CTLA4 BsAb 5mg/kg iv Q2W for 2nd treatment; cohort 2 enrolled subjects receiving PD-L1/CTLA4 BsAb in combination with gemcitabine/albumin- paclitaxel as 1st treatment for 4-6 cycles with PD-L1/CTLA4 BsAb monotherapy maintainence; cohort 3 enrolled subjects received systemic chemotherapy, receiving PD-L1/CTLA4 BsAb combined with oxaliplatin / irinotecan / leucovorin / fluorouracil (FOLFIRINOX) as 1st treatment for 4-6 cycles withPD-L1/CTLA4 BsAb monotherapy maintainence; until disease progression according to RECIST 1.1, intolerable toxicity, withdrawal, death, 2-yr treatment,who comes first. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04324307
Study type Interventional
Source Changhai Hospital
Contact Shiwei Guo, Doctor
Phone 86-18621500666
Email gestwa@163.com
Status Recruiting
Phase Phase 1/Phase 2
Start date November 26, 2019
Completion date November 2023

See also
  Status Clinical Trial Phase
Completed NCT00910741 - NC-6004(Nanoplatin) and Gemcitabine to Treat Pancreatic Cancer in Asia Phase 1/Phase 2