Viewing Study NCT02675478



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Last Modification Date: 2024-10-26 @ 11:56 AM
Study NCT ID: NCT02675478
Status: COMPLETED
Last Update Posted: 2019-02-12
First Post: 2016-02-02

Brief Title: Phase 1 Study of Quizartinib
Sponsor: Daiichi Sankyo Co Ltd
Organization: Daiichi Sankyo

Study Overview

Official Title: A Phase 1 Open-Label Dose Escalation Study of Quizartinib An Oral FLT3 Inhibitor in Japanese Patients With Relapsed or Refractory Acute Myeloid Leukemia
Status: COMPLETED
Status Verified Date: 2018-11
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: This is a dose escalation study to evaluate the safety tolerability and pharmacokinetics of quizartinib for Japanese acute myeloid leukemia AML subjects
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?: True
Is an FDA AA801 Violation?: None