Ignite Creation Date:
2024-05-05 @ 9:52 PM
Last Modification Date:
2024-10-26 @ 10:11 AM
Study NCT ID:
NCT00989261
Status:
COMPLETED
Last Update Posted:
2019-12-11
First Post:
2009-10-01
Brief Title:
Efficacy Study for AC220 to Treat Acute Myeloid Leukemia AML
Sponsor:
Daiichi Sankyo
Organization:
Daiichi Sankyo
Study Overview
Official Title:
Phase 2 Open-Label AC220 Monotherapy Efficacy ACE Study in Patients With Acute Myeloid Leukemia AML With and Without FLT3-ITD Activating Mutations
Status:
COMPLETED
Status Verified Date:
2019-12
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:
ACE
Brief Summary:
AC220 will be administered as a once daily oral solution given continuously as 28-day treatment cycles without any rest periods until disease progression relapse intolerance to the drug or elective allogeneic hematopoietic stem cell transplantation HSCT
Detailed Description:
None
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
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 2009-013093-41 | EUDRACT_NUMBER | None | None |