Viewing Study NCT03727477



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Last Modification Date: 2024-10-26 @ 12:57 PM
Study NCT ID: NCT03727477
Status: COMPLETED
Last Update Posted: 2023-05-24
First Post: 2018-10-29

Brief Title: Efficacy of Treatment Sequences in Patients With Non-small Cell Lung Cancer Receiving Lorlatinib
Sponsor: Intergroupe Francophone de Cancerologie Thoracique
Organization: Intergroupe Francophone de Cancerologie Thoracique

Study Overview

Official Title: Efficacy of Treatment Sequences in Patients With ALK and ROS-1 Positive Non-small Cell Lung Cancer Who Received Lorlatinib as Part of the French Expanded Access Program
Status: COMPLETED
Status Verified Date: 2023-05
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: LORLATU
Brief Summary: The study will evaluate progression-free survival overall survival best response and duration of treatment in patients with advanced ALK- and ROS1-positive non-small cell lung cancer who received lorlatinib as part of the French expanded access program
Detailed Description: IFCT-1803 LORLATU study will evaluate progression-free survival overall survival best response and duration of treatment in patients with advanced ALK- and ROS1-positive non-small cell lung cancer who received lorlatinib PF-06463922 as part of the French expanded access program Those outcomes will be correlated to clinical pathological and radiological characteristics of patients

Study Oversight

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