Viewing Study NCT04775446



Ignite Creation Date: 2024-05-06 @ 3:50 PM
Last Modification Date: 2024-10-26 @ 1:58 PM
Study NCT ID: NCT04775446
Status: COMPLETED
Last Update Posted: 2022-02-04
First Post: 2021-02-01

Brief Title: Evaluation of the ClinicalBiological Characteristics Efficacy and Safety of Patients With Malignant Pleural Mesothelioma Treated by Immunotherapy
Sponsor: Centre Hospitalier Intercommunal Creteil
Organization: Centre Hospitalier Intercommunal Creteil

Study Overview

Official Title: Multicentre Observational Study Evaluating the ClinicalBiological Characteristics Efficacy and Safety of Patients With Malignant Pleural Mesothelioma Treated by Immunotherapy in Real Life Setting
Status: COMPLETED
Status Verified Date: 2022-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: MESOIMMUNE
Brief Summary: The objective of this multicentre descriptive analysis is to describe the clinical and biological characteristics of patients who have received Programmed cell death 1 anti-PD1 PDL1 Programmed death-ligand 1 PDL1 immunotherapy outside of a clinical trial in terms of efficacy and safety
Detailed Description: Immunotherapy is now an option in the treatment of malignant pleural mesothelioma A French study Mesothelioma Avastin plus Pemetrexed-cisplatin Study 2 MAPS 2 prospective in 2nd line or more found 40 and 52 disease control rate with respectively an anti-PD1 antibody or a combo of anti-PD1 and Cytotoxic T-Lymphocyte-Associated protein 4 anti-CTLA4 Safety was rather good with 14 and 26 grade 3-4 in the Nivolumab and combo group respectively

Thanks to this trial and data from the literature Programmed cell death 1 anti-PD1 PDL1 Programmed death-ligand 1 PDL1 immunotherapy became an option in the treatment of malignant pleural mesothelioma after validation by a multidisciplinary meeting

The objective of this multicentre descriptive analysis is to describe the clinical and biological characteristics of patients who have received anti-PD1PDL1 immunotherapy outside of a clinical trial in terms of efficacy and safety

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None