Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06782451

Development of Preclinical Models Derived From Tumors With a Molecular Abnormality of Interest to Test Their Sensitivity to New Anti-tumor Therapies.

Led by Centre Antoine Lacassagne · Updated on 2025-09-29

50

Participants Needed

1

Research Sites

269 weeks

Total Duration

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AI-Summary

What this Trial Is About

This study aims to collect tumor samples from patients carrying a mutation of interest to develop a cell culture technique for "spheroids. The goal is to use these spheroids to model responses to anticancer treatments. Various therapeutic molecules can be tested on these spheroids, enabling the evaluation of the potential of new molecules or the activity of existing ones specifically on the tumor (bearing the mutation of interest) from which the spheroid was developed. Tumor samples will be collected as part of biopsies or surgeries conducted during routine patient care.

CONDITIONS

Official Title

Development of Preclinical Models Derived From Tumors With a Molecular Abnormality of Interest to Test Their Sensitivity to New Anti-tumor Therapies.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older.
  • Patient with at least one mutation of interest identified by the investigator.
  • Patient with a malignant tumor at a locally advanced or metastatic stage.
  • Scheduled tumor tissue sample collection via surgery, radiology, or endoscopy as part of standard care.
  • Tumor volume sufficient for analysis and transfer to the research laboratory.
  • INR less than 1.5; Platelets greater than 50,000/µL.
  • Patient informed about the study and has signed the informed consent form.
  • Patient affiliated with social security insurance.
Not Eligible

You will not qualify if you...

  • Patient with multiple primary malignant tumors.
  • Known infection with HIV, Hepatitis B, or Hepatitis C.
  • Use of certain blood-thinning medications without possibility of suspension before the procedure (including Clopidogrel, Prasugrel, Ticlopidine, low molecular weight heparin, Fondaparinux, Abciximab, Eptifibatide, Tirofiban, Argatroban, Bivalirudin, Dabigatran etexilate).
  • Patient considered vulnerable, including pregnant or breastfeeding women, individuals deprived of liberty, hospitalized without consent, or adults under legal protection unable to consent.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Centre Antoine Lacassagne

Nice, France, 06189

Actively Recruiting

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Research Team

S

Study coordinator

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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