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Study identifier: NCT07124858 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingCOFRUQ

Prospective National Cohort Evaluating Prognostic Factors for Efficacy of Fruquintinib Treatment in Patients With Metastatic Colorectal Cancer

Condition: Metastatic Colorectal Cancer (CRC) · Antineoplastic Agents, Immunological · VEGFR-TKI  ·  Sponsor: Federation Francophone de Cancerologie Digestive

PhaseNA
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where83 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The main objective of this study is to identify the prognostic factors (clinico-biological) for the efficacy (overall survival) of fruquintinib in patients with metastatic colorectal cancer.

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

Talk to the study team

Contact details are listed per location below or on the registry record.

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Patients aged 18 and over. * Histologically confirmed colorectal adenocarcinoma with locally advanced disease and/or unresectable metastasis(es) receiving treatment with fruquintinib under i) compassionate/early access and ii) marketing authorisation and reimbursement in France. * Obtain informed consent from the patient for the clinical-biological cohort. * Agreement to take biological samples of ctDNA and send tumour blocks (patient participation in the pharmacokinetic study remains optional). Exclusion Criteria: * Patient with another concurrent cancer at the time of diagnosis, requiring systemic treatment or influencing prognosis (in the opinion of the centre's medical team). * Contraindication due to psychological or social reasons that may hinder follow-up (cognitive deficit, psychological disorders incompatible with obtaining consent; inability to be followed in the same centre throughout the follow-up period for geographical reasons). * Pregnant or breast-feeding women. * Patients under court protection or subject to a protective measure (patient under guardianship or curatorship).

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (83)

Poitiers CHUPoitiers, France, FranceRecruiting
Centre HospitalierAlbi, FranceRecruiting
CHUAmiens, FranceRecruiting
Clinique de L EuropeAmiens, FranceRecruiting
Centre HospitalierAnnecy, FranceRecruiting
Centre HospitalierAurillac, FranceRecruiting
Centre HospitalierBayeux, FranceRecruiting
Centre HospitalierBayonne, FranceRecruiting
Centre HospitalierBeauvais, FranceRecruiting
CHUBesançon, FranceRecruiting
Centre Hospitalier Bethune BeuvryBeuvry, FranceRecruiting
Centre Pierre CurieBeuvry, FranceRecruiting

+ 71 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

PoitiersAlbiAmiensAnnecy

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