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NCT07165847

Neoadjuvant Radiotherapy Plus Tegafur, Oxaliplatin and Iparomlimab and Tuvonralimab in Resectable Gastric and GE-junction Cancer : A Randomized, Two-arm, Prospective Trial (TRIUNITE-05)

Recruiting now Phase 2 Last updated 10 September 2025
What this trial tests

Phase 2 trial testing Iparomlimab and Tuvonralimab in Immunotherapy in 40 participants. Currently enrolling.

Timeline
23 July 2025
Primary endpoint
23 September 2028
31 December 2030

Quick facts

Lead sponsorDaping Hospital and the Research Institute of Surgery of the Third Military Medical University
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment40
Start date23 July 2025
Primary completion23 September 2028
Estimated completion31 December 2030
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Daping Hospital and the Research Institute of Surgery of the Third Military Medical University

Who can join

18 and older, any sex, with Immunotherapy or Gastric Cancer (GC). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Neoadjuvant radiotherapy plus Tegafur, Oxaliplatin and Iparomlimab and Tuvonralimab in Resectable Gastric and GE-junction Cancer : A Randomized, Two-arm, Prospective Trial (TRIUNITE-05)

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Iparomlimab and Tuvonralimab

Trials testing the same drug.

Other recruiting trials for Immunotherapy

Currently open trials in the same condition.

Other Daping Hospital and the Research Institute of Surgery of the Third Military Medical University 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/NCT07165847.

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