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NCT07306273

IRE Combined With the Dual-Function Antibody PD-1/CTLA-4 for the Treatment of LAPC Following Failure of First-Line AG Therapy

Recruiting now Phase 2 Last updated 29 December 2025
What this trial tests

Phase 2 trial testing Irreversible electroporation in Pancreatic Adenocarcinoma Locally Advanced in 20 participants. Currently enrolling.

Timeline
15 December 2025
Primary endpoint
1 August 2027
1 August 2027

Quick facts

Lead sponsorRuijin Hospital
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date15 December 2025
Primary completion1 August 2027
Estimated completion1 August 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Ruijin Hospital

Who can join

18 and older, any sex, with Pancreatic Adenocarcinoma Locally Advanced. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study explores the efficacy and safety of irreversible electroporation(IRE) combined with the dual-function antibody PD-1/CTLA-4 (Apalulizumab) for the treatment of locally advanced pancreatic cancer following failure of first-line AG therapy. This research aims to accumulate more clinical evidence and treatment options for second-line therapy in locally advanced pancreatic cancer following failure of first-line regimen.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Irreversible electroporation

Trials testing the same drug.

Other recruiting trials for Pancreatic Adenocarcinoma Locally Advanced

Currently open trials in the same condition.

Other Ruijin Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07306273.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing