Status:

NOT_YET_RECRUITING

Lymphocyte Function Testing in Immuno-oncology

Lead Sponsor:

Centre Leon Berard

Conditions:

Immunotherapy

Advanced Solid Tumor Malignancies

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

Several studies have shown that the presence and levels of IFN-γ may correlate with better responses to immunotherapy. Higher baseline levels of IFN-γ and an increase in its production during treatmen...

Eligibility Criteria

Inclusion

  • Male or female aged 18 years or older with a confirmed diagnosis of solid tumors (any type of tumor) in advanced or metastatic stages
  • Patients who are due to start standard treatment with anti-PD1, anti-PDL1, or anti-CTLA4 (combinations of ICIs are permitted) at the Léon Bérard Center:
  • Cohort A: ICI without concomitant chemotherapy
  • Cohort B: ICI with concomitant chemotherapy
  • Patients who have understood, dated, and signed the consent form for this study before undergoing any protocol-specific procedures.
  • Patients affiliated with or covered by a social security system.

Exclusion

  • Patients to be treated with immunotherapy in combination with targeted therapy.
  • Patients treated with chemotherapy within the last 21 days prior to D1 of immunotherapy
  • Pregnant or breastfeeding patients.
  • Patients with other known cancers that are progressing or requiring the initiation of another treatment.
  • Patients with psychological, family, geographical, or social circumstances that, in the investigator's judgment, could potentially prevent the signing of an informed consent form and/or compliance with study procedures.
  • Patients in one or more of the following situations: subject to legal protection measures, deprived of liberty by judicial or administrative decision, receiving psychiatric care, admitted to a health or social care facility for purposes other than research

Key Trial Info

Start Date :

September 23 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 23 2025

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT07155811

Start Date

September 23 2025

End Date

September 23 2025

Last Update

September 4 2025

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