Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05088395

Analysis of Circulating Tumor mArkers in Blood 4 - ALCINA 4

Led by Institut Curie · Updated on 2026-04-14

2050

Participants Needed

2

Research Sites

471 weeks

Total Duration

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AI-Summary

What this Trial Is About

Multi-cohort exploratory prospective study. Participation in the ALCINA 4 study does not change the standard management of the patient, including the treatments administered. A sampling schedule will be set up for each cohort. Depending on the clinical context studied and the biomarkers studied and/or sought, the timing of blood samples will vary between cohorts. There may be up to 4 samples (or more) taken per patient for up to 18, 24 or 36 months. If a specific tumor sample is required, it will be collected only once during the study.

CONDITIONS

Official Title

Analysis of Circulating Tumor mArkers in Blood 4 - ALCINA 4

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient treated for cancer at one of the participating centers
  • 18 years old or higher
  • Signed informed consent form
  • Patient not deprived of their liberty or under guardianship (including temporary guardianship)
  • Patient covered by social security scheme
  • Patient with no compliance issue (related to geographical, social or psychological reasons) for study follow up
  • Other additional criteria will be defined (defining tumor type and clinical setting), by cohort
  • Tumor considered as accessible by biopsy (if biopsy is to be taken)
  • Normal blood coagulation tests (if applicable, and in case of a non-superficial tumor lesion)
  • No anticoagulant or antiaggregant treatment for the biopsy
Not Eligible

You will not qualify if you...

  • Pregnant and/or breast-feeding women depending on cohort

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Institut Curie

Paris, France, 75005

Actively Recruiting

2

Institut Curie

Saint-Cloud, France, 92210

Actively Recruiting

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Research Team

M

Marie-Emmanuelle LEGRIER

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

12

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