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Research Into Biomarkers Predictive of Survival and Response to Cancer Treatment (BEST)

C

Centre Antoine Lacassagne

Status

Enrolling

Conditions

Cancer

Treatments

Other: blood sampling

Study type

Interventional

Funder types

Other

Identifiers

NCT06851975
2018-61

Details and patient eligibility

About

Research into biomarkers predictive of survival and response to cancer treatment

Enrollment

40,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

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

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40,000 participants in 1 patient group

principal
Other group
Description:
blood sampling
Treatment:
Other: blood sampling

Trial contacts and locations

1

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Central trial contact

Victoria FERRARI, Dr

Data sourced from clinicaltrials.gov

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