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Clinical Trials in the USA / NCT04994795
Active, not recruiting Observational

Predictive Multimodal Signatures Associated With Response to Treatment and Prognosis of Patients With Stage IV Non-small Cell Lung Cancer

NCT04994795 · tracked via the Priya Life Science USA tracker
Sponsor
Sophia Genetics SAS
Phase
Observational
Started
2021-08-21
Last updated
2024-11-21

Condition(s) studied

Non-small Cell Lung Cancer Metastatic

Investigational drug(s) / intervention(s)

Predictive models (data collection)

Predictive models (data collection): Machine learning predictive models

Study summary

Predicting response to therapy and disease progression in stage IV NSCLC patients treated with pembrolizumab monotherapy, chemotherapy-pembrolizumab combination therapy or chemotherapy alone in the first-line setting.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Adult ≥18 years old * Patient diagnosed with Stage IV NSCLC (de novo or earlier stage progression to stage IV) * Absence of oncogene activating mutations eligible patients to targeted therapy (EGFR, ALK) * Cohort A: Received first line treatment with pembrolizumab monotherapy * Cohort B: Received first line treatment with chemotherapy and pembrolizumab combination therapy * Cohort C: Received first line treatment with chemotherapy doublet Exclusion Criteria: * Prior anti-cancer therapy for actual stage IV NSCLC * Critical data missing (e.g., PD-L1 status, baseline millimetric imaging, first evaluation millimetric imaging) * Patients participating in other clinical trials that modify the standard of care

Primary outcome measure(s)

Trial sites (30)

FacilityCityRegionStatus
Holden Comprehensive Cancer Center at University of Iowa Health Care Iowa City Iowa
UMASS Memorial Health Worcester Massachusetts
Mayo Clinic Rochester Minnesota
Roswell Park Comprehensive Cancer Center Buffalo New York
Huntsman Cancer Institute Salt Lake City Utah
Carbone Comprehensive Cancer Center at University of Wisconsin Madison Wisconsin
DASA - Hospital Brasilia Brasília Brazil
DASA - Hospital de Niteroi Niterói Brazil
DASA - Hospital São Lucas Rio de Janeiro Brazil
DASA - Hospital Nove De Julho São Paulo Brazil
AC Camargo São Paulo Brazil
Sunnybrook Health Sciences Centre Toronto Toronto Canada
Avicenne Hospital Bobigny France
CHU Bordeaux Bordeaux France
Ambroise Paré Hospital Boulogne-Billancourt France
Hospices Civils de Lyon Lyon France
CHU de Nantes Nantes France
La Pitié Salpêtrière Paris France
Tenon Hospital Paris France
Foch Hospital Suresnes France
Centre Hospitalier de Toulon Toulon France
University Hospital Leipzig Leipzig Germany
Shaare Zadek Medical Center Jerusalem Israel
Sourasky Medical Center Tel Aviv Israel
University Hospital Of Parma Parma Italy
Policlinico Gemelli Roma Italy
Azienda Sanitaria Universitaria Friuli Centrale (ASU FC) Udine Italy
Fundacion jimenez diaz Madrid Spain
Puerta De Hierro Hospital Madrid Spain
Instituto Valenciano De Oncologia Valencia Spain
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04994795 on ClinicalTrials.gov ↗ ← All trials in the USA