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NCT06027775

Chemotherapy Alone Versus Chemotherapy Plus Targeted Therapy as Adjuvant Therapy for Initially Unresectable Colorectal Cancer Liver Metastases

Completed Last updated 7 September 2023
What this trial tests

trial testing Targeted agent in Colorectal Cancer Metastatic in 198 participants. Completed in 1 January 2023.

Timeline
1 January 2013
Primary endpoint
1 January 2023
1 January 2023

Quick facts

Lead sponsorFudan University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment198
Start date1 January 2013
Primary completion1 January 2023
Estimated completion1 January 2023

Drugs / interventions tested

Conditions studied

Sponsor

Fudan University

Who can join

Adults 18 to 75, any sex, with Colorectal Cancer Metastatic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Chemotharapy plus targeted therapy regimen, as an adjuvant therapy, can effectively reduce the rate of both intrahepatic and extrahepatic recurrence in initially unresectable CRLM patients. Those with KRAS/NRAS/BRAF mutated tumors or cycle of conversion therapy ≤ 4 can benefit more from chemotharapy plus targeted therapyrather than from chemotharapy alone, with a tolerable toxicity profile.

Publications & conference data

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

  1. Chemotherapy alone versus chemotherapy plus targeted therapy as adjuvant therapy for initially unresectable colorectal cancer liver metastases: a multicenter cohort study.
    Chang W, Zhou S, Guan X, Xu D, et al · · 2025 · PMID 41282550 · DOI 10.1093/gastro/goaf098

Verify or expand the search:

Other recruiting trials for Colorectal Cancer Metastatic

Currently open trials in the same condition.

Other Fudan University trials

Trials by the same sponsor.

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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/NCT06027775.

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