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NCT06157216

Minimal Residual Disease-guided Adjuvant Therapy for Gastric Cancer

Active, enrolled NA Last updated 7 January 2025
What this trial tests

NA trial testing MRD-guided therapy in Stage II-III Gastric Cancer in 85 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 October 2023
Primary endpoint
1 April 2027
1 April 2029

Quick facts

Lead sponsorQilu Hospital of Shandong University
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment85
Start date1 October 2023
Primary completion1 April 2027
Estimated completion1 April 2029
Sites5 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Qilu Hospital of Shandong University

Who can join

Adults 18 to 75, any sex, with Stage II-III Gastric Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a multicenter, single-arm, interventional study to explore the feasibility of circulating tumor DNA (ctDNA)-MRD testing to guide postoperative adjuvant treatment strategies in patients with stage II-III gastric cancer.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Japan society of clinical oncology position paper on appropriate clinical use of molecular residual disease (MRD) testing.
    Kobayashi S, Nakamura Y, Hashimoto T, Bando H, et al · · 2025 · cited 6× · PMID 39920551 · DOI 10.1007/s10147-024-02683-0

Verify or expand the search:

Other recruiting trials for Stage II-III Gastric Cancer

Currently open trials in the same condition.

Other Qilu Hospital of Shandong 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/NCT06157216.

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