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RecruitingNCT06851975BESTUpdated May 29, 2026

Research Into Biomarkers Predictive of Survival and Response to Cancer Treatment

An observational study in Cancer, sponsored by Centre Antoine Lacassagne. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-29.

Sponsored by Centre Antoine Lacassagne · Observational

From the registry’s dates

  • Started Jan 2020; still recruiting 6 years 10 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
40,000
Ages
18 Years and older
Sex
All
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Study summary

Research into biomarkers predictive of survival and response to cancer treatment

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Conditions studied

  • Cancer

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In context

Neoplasms

10,818 studies on the registry are indexed under Neoplasms; 2,324 are open to participants now.

This study's planned enrollment of 40,000 is above the median of 200 across 2,638 observational studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

Centre Antoine Lacassagne is the lead sponsor of 66 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with cancer receiving care at Centre Antoine Lacassagne are prospectively recruited for biospecimen collection during routine clinical blood sampling.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient having a blood test, venous line insertion or injection on an implantable venous device scheduled as part of their standard care,
  • Patient who has read the information note and stated that he/she has no objections
  • Patient who has not objected to the use of this data for medical research purposes
  • Patient with social security cover.

Exclusion criteria

Exclusion Criteria:

  • Patient already included in the study
  • Patient considered to be a vulnerable person; vulnerable persons are defined in article L1121-5 to -8
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
40,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • principal

    blood sampling

    Other: blood sampling

Interventions

  • Otherblood sampling

    36ml of blood will be taken during a blood sampling performed in standard practice

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What researchers measure

Primary outcomes

  1. Prediction

    The aim of this project is to make a biobank in prevision of MR004 sub-projects which define specific biomarkers studied to identify biomarkers predictive of response.

    Time frame: day 1

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: Yes — pseudonymised data will only be collected

Supporting information: Study protocol, Clinical study report

Time frame: at the end of study

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06851975
Lead sponsor
Centre Antoine Lacassagne
Responsible party
Sponsor
First posted
Feb 28, 2025
Start date
Jan 7, 2020
Primary completion
Dec 31, 2099 (estimated)
Completion
Dec 31, 2099 (estimated)
Last update
May 29, 2026

Study contacts

Victoria FERRARI, Dr
Contact
victoria.ferrari@nice.unicancer.fr
+33 492031311

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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