Viewing Study NCT02926586



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Last Modification Date: 2024-10-26 @ 12:11 PM
Study NCT ID: NCT02926586
Status: COMPLETED
Last Update Posted: 2022-05-11
First Post: 2016-10-05

Brief Title: Fludarabine and Cytarabine Versus High-dose Cytarabine for CBF-AML
Sponsor: Shanghai General Hospital Shanghai Jiao Tong University School of Medicine
Organization: Shanghai General Hospital Shanghai Jiao Tong University School of Medicine

Study Overview

Official Title: Fludarabine and Cytarabine Versus High-dose Cytarabine in Consolidation Treatment of Core-bing Factor Acute Myeloid Leukemia A Prospective Multicenter Randomized Study
Status: COMPLETED
Status Verified Date: 2024-09
Last Known Status: RECRUITING
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 the study is to determine whether Fludarabine in combination with cytarabine is more effective than high-dose cytarabine in post-remission therapy for patients with core-binding factor acute myeloid leukemia
Detailed Description: The recurrence rate relapse-free survival rate and overall survival rate of CBF-AML patients were compared between FA and HIDAC regimens Observe the prognostic value of factors such as c-KIT gene mutation and minimal residual disease MRD

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