Viewing Study NCT01459159


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Study NCT ID: NCT01459159
Status: TERMINATED
Last Update Posted: 2013-11-25
First Post: 2011-10-11
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Study of (Telintra®) in Non-Del(5q) Myelodysplastic Syndrome
Sponsor: Telik
Organization:

Study Overview

Official Title: Phase 2b Study of Oral Ezatiostat Hydrochloride (Telintra®) in Patients With Low to Intermediate-1 Risk, Non-Deletion 5q Myelodysplastic Syndrome
Status: TERMINATED
Status Verified Date: 2013-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Study TLK199.2108 was terminated for business reasons.
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a multicenter, single arm open label Phase 2b Study of oral ezatiostat (Telintra®) in Patients who are RBC tranfusion dependent, Low to INT-1 IPSS risk, non-del (5q) Myelodysplastic Syndrome (MDS).
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?: