← Eichor
Study identifier: NCT06346197 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Combination of Immune Checkpoint in Locally Advanced or Metastatic MSI/dMMR Esogastric Adenocarcinomas

Condition: Gastric Cancer · MSI-H · Metastatic Cancer  ·  Sponsor: Centre Leon Berard

PhasePhase 3
Planned participants132
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

CIME is a multicenter, randomised, comparative, open-label phase III study aiming to compare the survival of patients suffering from MSI-H/dMMR locally advanced or metastatic oeasogastric adenocarcinoma treated by a bi-immunotherapy (experimental arm) versus standard current treatment (FOLFOX/XELOX + nivolumab : standard arm).

This description comes directly from the study's public registry record.

Talk to the study team

Christelle DE LA FOUCHARDIERE, MD  ·  04 91 22 35 03  ·  delafouchardierec@ipc.unicancer.fr

Always discuss trial participation with your own doctor first.

Locations (7)

CHU de BrestBrest, FranceRecruiting
CHU de Clermont-FerrandClermont-Ferrand, FranceRecruiting
Centre Léon BérardLyon, FranceRecruiting
Hôpital Privé Jean MermozLyon, FranceRecruiting
Institut Paoli CalmettesMarseille, FranceRecruiting
Institut Mutualiste MontsourisParis, FranceRecruiting
CHU de PoitiersPoitiers, FranceRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06346197