Extended Evaluation of Deferasirox Film-coated Tablet (FCT) Formulation
NCT02720536 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 53
Last updated 2020-03-03
Summary
Extend evaluation of deferasirox film-coated tablet (FCT) formulation
Conditions
- Chronic Iron Overload
Interventions
- DRUG
-
Deferasirox
Deferasirox FCT will be provided as 90 mg, 180 mg and 360 mg film-coated tablets for oral use.
Sponsors & Collaborators
- lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 10 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-08-16
- Primary Completion
- 2019-07-23
- Completion
- 2019-07-23
Countries
- Austria
- Greece
- Italy
Study Locations
More Related Trials
-
Study With Deferiprone and/or Desferrioxamine in Iron Overloaded Patients
NCT00350662 ·Status: COMPLETED ·Phase: PHASE3
-
Study of Deferasirox for Treatment of Transfusional Iron Overload in Myelodysplastic Patients
NCT00110266 ·Status: COMPLETED ·Phase: PHASE2
-
Phase I Study to Examine the Effect of Deferasirox on Renal Hemodynamics in β-thalassemia Patients With Transfusional Iron Overload
NCT00560820 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Efficacy and Safety of Deferasirox Film-coated Tablet Versus Phlebotomy in Patients With Hereditary Hemochromatosis (HH)
NCT03203850 ·Status: TERMINATED ·Phase: PHASE2
-
Safety and Efficacy of Desferasirox in Chinese Patients With Iron Overload and Aplastic Anemia
NCT01546415 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluating Use of Deferasirox as Compared to Deferoxamine in Treating Cardiac Iron Overload
NCT00600938 ·Status: COMPLETED ·Phase: PHASE2
-
Open-label, Multicenter Study Assessing Preference for Deferasirox Film-coated Tablet Compared to Dispersible Tablet
NCT02993224 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Deferasirox in Combination With Deferoxamine Followed by Deferasirox Monotherapy in Severe Cardiac Iron Overload
NCT01254227 ·Status: COMPLETED ·Phase: PHASE2
-
Evaluating the Efficacy of Deferasirox in Transfusion Dependent Chronic Anaemias (Myelodysplastic Syndrome, Beta-thalassaemia Patients) With Chronic Iron Overload
NCT00564941 ·Status: COMPLETED ·Phase: PHASE4
-
Extension Study of Iron Chelation Therapy With Deferasirox in β-thalassemia and Rare Chronic Anemia Patients
NCT00303329 ·Status: COMPLETED ·Phase: PHASE2
-
Safety of ICL670 vs. Deferoxamine in Sickle Cell Disease Patients With Iron Overload Due to Blood Transfusions
NCT00067080 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Deferasirox Relative to Subcutaneous Deferoxamine in Sickle Cell Disease Patients
NCT00110617 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Deferasirox in Iron Overload From Beta-thalassemia Unable to be Treated With Deferoxamine or Chronic Anemias
NCT00061763 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Deferasirox in Non-transfusion Dependent Thalassemia Patients With Iron Overload and a One Year Open-label Extension Study
NCT00873041 ·Status: COMPLETED ·Phase: PHASE2
-
Effect of Deferasirox on Patients With Cardiac MRI T2* < 20 Msec
NCT00879242 ·Status: COMPLETED ·Phase: PHASE2
-
Cardiac T2* in Beta-thalassemia Patients on Deferasirox Treatment
NCT00447694 ·Status: COMPLETED ·Phase: PHASE2
-
A Study of Iron Oligosaccharide in CHF Patients
NCT00537186 ·Status: COMPLETED ·Phase: PHASE3
-
An Extension Study of Iron Chelation Therapy With Deferasirox (ICL670) in β-thalassemia Patients With Transfusional Iron Overload
NCT00171210 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy of Deferasirox in Combination With Desferoxamine in β-thalassaemia Patients With Severe Cardiac Iron Overload
NCT01459718 ·Status: TERMINATED ·Phase: PHASE2
-
Evaluation of the Safety, Tolerability, Pharmacokinetics (PK) and Effects on Liver Iron Concentration of ICL670 Relative to Deferoxamine(DFO).
NCT01090323 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Acceptability of Deferiprone Delayed Release Tablets in Patients With Systemic Iron Overload
NCT03802916 ·Status: COMPLETED ·Phase: PHASE2
-
Extension Study of the Efficacy and Safety of Deferasirox Treatment in Beta-thalassemia Patients With Transfusional Hemosiderosis (Study Amended to 2-year Duration)
NCT00171301 ·Status: COMPLETED ·Phase: PHASE4
-
Deferasirox in Treating Patients With Very Low, Low, or Intermediate-Risk Red Blood Cell Transfusion Dependent Anemia or Myelodysplastic Syndrome
NCT02943668 ·Status: TERMINATED ·Phase: PHASE2
-
Efficacy and Safety of Oral Deferasirox (20 mg/kg/d) in Pts 3 to 6 Months After Allogeneic Hematopoietic Cell Transplantation Who Present With Iron Overload
NCT00654589 ·Status: COMPLETED ·Phase: PHASE4
-
Expanded Access of Deferasirox to Patients With Congenital Disorders of Red Blood Cells and Chronic Iron Overload
NCT00235391 ·Status: COMPLETED ·Phase: PHASE3