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Study details
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Chemotherapy + Anakinra in Patients With Pancreatic Adenocarcinoma (PDAC)

Baylor Research Institute
NCT IDNCT04926467ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

24

Study length

about 5.9 years

Ages

18+

Locations

1 site in TX

About this study

This trial is testing a treatment called anakinra, which is an anti-inflammatory medication, when combined with chemotherapy for people who have pancreatic adenocarcinoma. The goal is to see if adding anakinra improves outcomes for these patients.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Anakinra
PhasePhase 2
DrugAnakinra

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

anakinra

Endpoints

Secondary: To describe the effect of anakinra in combination with perioperative chemotherapy on the prevalence and severity of pain by monitoring patients' pain level using memorial pain assessment card (MPAC)., To determine the effect of anakinra in combination with perioperative chemotherapy on overall survival (OS) of PDAC patients. A benchmark of 24 months OS will be used to determine how many patients meet or exceed this goal., To determine the effect of anakinra in combination with perioperative chemotherapy on patients' health-related quality of life by monitoring patients using EORTC quality of life survey questionnaire (EORTC QLQ-C30)., To determine the effect of anakinra in combination with perioperative chemotherapy on response rate, To determine the effect of anakinra in combination with perioperative chemotherapy on the inflammasomes ( IL6, CRP, IL1α and IL1β) in blood and in the resected pathology specimens., To determine the effect of anakinra in combination with perioperative chemotherapy on the median disease free survival (DFS). A benchmark of 12 months DFS will be used to determine how many patients meet or exceed this goal.