Viewing Study NCT00171821



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00171821
Status: COMPLETED
Last Update Posted: 2020-02-11
First Post: 2005-09-13

Brief Title: A Study Assessing the Efficacy and Safety of Deferasirox in Patients With Transfusion-dependent Iron Overload
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: A One Year Open-label Single-arm Multi-center Trial Evaluating the Efficacy and Safety of Oral ICL670 20 mgkgDay in Patients Diagnosed With Transfusion-dependent Iron Overload
Status: COMPLETED
Status Verified Date: 2013-06
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 study uses a single arm multi-center open-label trial design The study will assess the efficacy and safety of 52 weeks of treatment with deferasirox ICL670 in patients with evidence of transfusion induced iron overload
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
2004-003953-16 EUDRACT_NUMBER None None