Cliniques Universitaires Saint-Luc
Brussels, 1200, Belgium
NCT Number: NCT03125603
The immune-related adverse events (irAEs) linked to the important activation of the immune system by new immunotherapy treatments in patients affected by Non-small-cell lung carcinoma (NSCLC) have not received a lot of systematic study or been monitored over time outside of clinical trials.
This study aims to verify, on the basis of the data collected in a prospective and retrospective manner, that the side-effects due of anti-PD-(L)-1 or anti-CTLA-4 treatments observed in the target population of the controlled clinical trials are the same as in the general clinical population.
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Notify Me20 year–85 year
All sexes
Observational
Brussels, 1200, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Gradation of the adverse events according to CTCAE scale 4.03 (June 2010).
Time frame: Through study completion, an average of 20 months.
Census of the side-effect type, severity according to the CTCAE and monitoring the side-effect's development.
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Other
Census and Follow-up of the Side Effects in the New Immunotherapeutic Treatments Anti-PD-(L)-1 and Anti-CTLA-4 of the Non Small Cells Lung Cancer
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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