Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05813418

Identification of Predictive Biomarkers for Immune-Related Adverse Events (irAEs) in Patients Undergoing Immune CheckPoint Inhibitors (ICPI) Treatment

Identification of Predictive Biomarkers for Immune-Related Adverse Events (irAEs) in Patients

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Centre Hospitalier Universitaire, Amiens · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In the last decades, cancer treatment was based on surgery, radiotherapy and chemotherapy. Recently, treatments have largely evolved, first with targeted therapies (notably tyrosin kinase inhibitors, TKI) and then with immune checkpoint inhibitors (ICPI, notably anti-CTLA-4 and anti- PD1). The last ones can induce durable anti-tumoral responses in patients, even if metastases are present. Their mechanisms of action are focused on the activation of immune system in order to eliminate the tumor. ICPI, because of their mechanisms of action, target immune tolerance key components and can induce important immune toxicities (colitis, hepatitis, dermatitis, thyroiditis ...), leading to early discontinuation of treatment, severe or chronic morbidity, and can sometimes be lethal. It is of importance to detect patient at risk of irAEs, because of the increasing use of ICPI and the long- term response capacity in treated patients.

Conditions

Interventions

TypeNameDescription
BIOLOGICALblood retriewalblood retriewal for cytokine concentration measurement

Timeline

Start date
2021-07-02
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2023-04-14
Last updated
2025-06-04

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05813418. Inclusion in this directory is not an endorsement.