Viewing Study NCT04111705



Ignite Creation Date: 2024-05-06 @ 1:46 PM
Last Modification Date: 2024-10-26 @ 1:19 PM
Study NCT ID: NCT04111705
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-03-07
First Post: 2019-08-30

Brief Title: Lorlatinib After Failure of First-line Second-generation ALK Kinase Inhibitor in Patients with Advanced ALK-positive Non-small Cell Lung Cancer
Sponsor: Intergroupe Francophone de Cancerologie Thoracique
Organization: Intergroupe Francophone de Cancerologie Thoracique

Study Overview

Official Title: A Phase II Non-randomized Single Group Assignment Open-label Multicenter Study of Efficacy and Safety of Lorlatinib Monotherapy After Failure of First-line Second-generation ALK Kinase Inhibitor in Patients with Advanced ALK-positive Non-small Cell Lung Cancer
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-03
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: ORAKLE
Brief Summary: Crizotinib is a first-generation ALK tyrosine kinase inhibitor ITK-ALK It is the standard first-line treatment for patients with advanced NSCLC with ALK gene rearrangement Alectinib ceritinib and brigatinib are second-generation ITK-ALK They have been shown to be effective in the first line of treatment in randomized trials Alectinib has shown superiority to crizotinib as the first line of treatment in three randomized therapeutic trials positioning this ITK-ALK as the treatment of choice in first-line treatment Despite the effectiveness of these new treatments all patients will virtually experience a relapse There is no data on second-generation TKI-ALK resistance mechanisms when given as first-line treatment and the best therapeutic strategy for progression is undefined
Detailed Description: None

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