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Recruiting NCT04300062

NCT04300062 Tumor Rebiopsy During Progression Under Immunotherapy for Patients With Lung Cancer

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Clinical Trial Summary
NCT ID NCT04300062
Status Recruiting
Phase
Sponsor Assistance Publique - Hôpitaux de Paris
Condition Lung Cancer
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2020-08-18
Primary Completion 2027-08

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Rebiopsy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2020-08-18 with a primary completion date of 2027-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The objective of the study aims to collect tumor tissue at the moment of progression under Immune checkpoint inhibitors (ICI) in biological resources center in Ambroise Paré hospital, in order to insure later study on molecular mechanism involving the progression of NSCLC and SCLC under ICI. The further analysis of research will be performed in the EA 4340 unity, Biomarkers and Clinical Trials in cancerology and onco-hematology, UVSQ, University of Paris-Saclay.

Eligibility Criteria

Inclusion Criteria: * Diagnosed NSCLC or SCLC; * Patient treated priorly by ICI and progressed under ICI; * Have provided written informed consent for the study; * Be \>/= 18 years of age on day of signing informed consent. Exclusion Criteria: * Patient under guardianship or curatorship; * Unable to provide written informed consent for the study; * Technical impossibility to carry out tissular rebiopsy under local anesthesia.

Contact & Investigator

Central Contact

Etienne Giroux Leprieur, MD, PhD

✉ etienne.giroux-leprieur@aphp.fr

📞 +33 1 49 09 58 02

Principal Investigator

Etienne Giroux Leprieur, MD, PhD

PRINCIPAL INVESTIGATOR

Service de Pneumologie et Oncologie thoracique, Hôpital Ambroise Paré, APHP

Frequently Asked Questions

Who can join the NCT04300062 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Lung Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04300062 currently recruiting?

Yes, NCT04300062 is actively recruiting participants. Contact the research team at etienne.giroux-leprieur@aphp.fr for enrollment information.

Where is the NCT04300062 trial being conducted?

This trial is being conducted at Boulogne-Billancourt, France.

Who is sponsoring the NCT04300062 clinical trial?

NCT04300062 is sponsored by Assistance Publique - Hôpitaux de Paris. The principal investigator is Etienne Giroux Leprieur, MD, PhD at Service de Pneumologie et Oncologie thoracique, Hôpital Ambroise Paré, APHP. The trial plans to enroll 50 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology