Actively Recruiting
Observational Multicenter Study in Patients Receiving Chemotherapy and Amivantamab for Metastatic Non-small Cell Lung Cancer
Led by GFPC Investigation · Updated on 2026-05-01
100
Participants Needed
16
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this observational study is to understand how well a treatment combining chemotherapy and amivantamab works in real life, and how safe it is, in adults with metastatic non-small cell lung cancer (NSCLC) who have certain EGFR gene mutations. The study includes two groups of people: * Group A: people with an EGFR exon 20 insertion who receive amivantamab together with platinum-based chemotherapy as their first treatment, through an early access program. * Group B: people with an EGFR exon 19 or exon 21 mutation who receive amivantamab with platinum-based chemotherapy after having been treated with osimertinib (with or without chemotherapy), also through an early access program. The main question the study wants to answer is: How long can the combination of amivantamab and chemotherapy keep the cancer from coming back or getting worse in these two groups of people? People already receiving amivantamab and chemotherapy for NSCLC through an early access program may be included. They will continue to be followed by their usual oncologist as part of their normal medical care. The study will simply collect their medical information from March 21, 2024 to October 21, 2025. No extra tests or procedures are required. This is an observational study, carried out by the GFPC and partner centers in France.
CONDITIONS
Official Title
Observational Multicenter Study in Patients Receiving Chemotherapy and Amivantamab for Metastatic Non-small Cell Lung Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient over 18 years old
- For Cohort A: Metastatic NSCLC with EGFR exon 20 insertion treated with amivantamab and platinum-based chemotherapy as first-line therapy through an early access program
- For Cohort B: Metastatic NSCLC with EGFR exon 19 or 21 mutation treated with amivantamab and platinum-based chemotherapy after osimertinib (with or without chemotherapy) through an early access program
- Patient covered by the French National Health Insurance system or an approved third-party payer
- Patient does not object to collection of personal data for research purposes
You will not qualify if you...
- Patient under legal guardianship or with a protective legal measure
- Patient who explicitly refuses collection or use of personal data for research
- Patient not enrolled, managed, or followed by a qualified investigator at the study site
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 16 locations
1
CH du Pays d Aix - Service des Maladies Respiratoires
Aix-en-Provence, France, 13616
Actively Recruiting
2
APHP Hôpital Avicennes
Bobigny, France, 93000
Actively Recruiting
3
Hôpital Louis Pradel
Bron, France, 69500
Active, Not Recruiting
4
Pneumologie Centre François Baclesse
Caen, France, 14000
Active, Not Recruiting
5
Pneumologie Centre Hospitalier Intercommunal de Créteil
Créteil, France, 94010
Actively Recruiting
6
Hôpital A. Mignot
Le Chesnay, France, 78157
Actively Recruiting
7
Pneumologie Hôpital Calmette
Lille, France, 59000
Actively Recruiting
8
Pneumologie Hôpital privé Jean Mermoz
Lyon, France, 69085
Actively Recruiting
9
Centre Léon Bérard
Lyon, France, 69373
Actively Recruiting
10
Hôpital Nord
Marseille, France, 13915
Actively Recruiting
11
CHRU de Nancy
Nancy, France, 54000
Active, Not Recruiting
12
Centre Antoine Lacassagne
Nice, France, 06149
Active, Not Recruiting
13
Institut Curie
Paris, France, 75005
Active, Not Recruiting
14
CH de la Région d'Annecy - Service de Pneumologie
Pringy, France, 74374
Actively Recruiting
15
Pneumologie CHU St Etienne
Saint-Etienne, France, 42270
Actively Recruiting
16
CHU La Réunion Site Sud
Saint-Pierre, France, 97410
Actively Recruiting
Research Team
P
Prof. Laurent Greillier
CONTACT
S
Soizic Ferlandin
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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