Viewing Study NCT00750334


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Study NCT ID: NCT00750334
Status: TERMINATED
Last Update Posted: 2015-05-21
First Post: 2008-09-09
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Study of Oral Clofarabine in Adult Patients With Myelodysplastic Syndromes (MDS)
Sponsor: Genzyme, a Sanofi Company
Organization:

Study Overview

Official Title: A Phase I, Open-Label, Dose-Finding and Food Effect Study of Oral Clofarabine in Previously Treated Adult Patients With Myelodysplastic Syndromes (MDS)
Status: TERMINATED
Status Verified Date: 2015-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Terminated to focus on comparable trial, CLOMDS02507
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study will be used to determine the maximum tolerated dose of oral clofarabine when administered daily for 14 consecutive days repeated every 21 days.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: