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Study identifier: NCT05813418 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Immunotherapy · Immune Checkpoint Inhibitors · Immune-related Adverse Event  ·  Sponsor: Centre Hospitalier Universitaire, Amiens

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Gwladys BOURDENET, DR  ·  03.22.08.70.72  ·  bourdenet.gwladys@chu-amiens.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU Amiens PicardieAmiens, Picardie, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05813418