Viewing Study NCT03194893



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Last Modification Date: 2024-10-26 @ 12:26 PM
Study NCT ID: NCT03194893
Status: RECRUITING
Last Update Posted: 2024-07-11
First Post: 2017-06-20

Brief Title: A Rollover Study of Alectinib in Patients With Anaplastic Lymphoma Kinase ALK-Positive or Rearranged During Transfection RET-Positive Cancer
Sponsor: Hoffmann-La Roche
Organization: Hoffmann-La Roche

Study Overview

Official Title: A Multicenter International Rollover Study of Alectinib in Patients With Anaplastic Lymphoma Kinase ALK-Positive or Rearranged During Transfection RET-Positive Cancer
Status: RECRUITING
Status Verified Date: 2024-10
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: None
Brief Summary: The purpose of this study is to provide continued treatment with alectinib or crizotinib as applicable to participants with ALK- or RET positive cancer who were previously enrolled in any Roche-sponsored alectinib study and who are deriving continued clinical benefit from alectinib or crizotinib in the parent trial at the time of parent trial closure
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
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
Secondary IDs
Secondary ID Type Domain Link
2017-000207-24 EUDRACT_NUMBER None None