Success Metrics

Clinical Success Rate
82.4%

Based on 42 completed trials

Completion Rate
82%(42/51)
Active Trials
1(2%)
Results Posted
69%(29 trials)
Terminated
9(15%)

Phase Distribution

Ph phase_4
14
23%
Ph not_applicable
3
5%
Ph phase_3
9
15%
Ph phase_2
25
41%
Ph phase_1
6
10%

Phase Distribution

6

Early Stage

25

Mid Stage

23

Late Stage

Phase Distribution57 total trials
Phase 1Safety & dosage
6(10.5%)
Phase 2Efficacy & side effects
25(43.9%)
Phase 3Large-scale testing
9(15.8%)
Phase 4Post-market surveillance
14(24.6%)
N/ANon-phased studies
3(5.3%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

75.0%

42 of 56 finished

Non-Completion Rate

25.0%

14 ended early

Currently Active

1

trials recruiting

Total Trials

61

all time

Status Distribution
Active(1)
Completed(42)
Terminated(14)
Other(4)

Detailed Status

Completed42
Terminated9
Withdrawn5
unknown4
Recruiting1

Development Timeline

Analytics

Development Status

Total Trials
61
Active
1
Success Rate
82.4%
Most Advanced
Phase 4

Trials by Phase

Phase 16 (10.5%)
Phase 225 (43.9%)
Phase 39 (15.8%)
Phase 414 (24.6%)
N/A3 (5.3%)

Trials by Status

completed4269%
withdrawn58%
recruiting12%
unknown47%
terminated915%

Recent Activity

Clinical Trials (61)

Showing 20 of 61 trialsScroll for more
NCT07023666Phase 2

Early Screening and Treatment of Heart Complication in Sickle Cell Disease

Recruiting
NCT04423237

Risk Factors and Measures to Prevent Liver and Pancreas Complications in Pediatric Patients After HSCT

Completed
NCT03387475Phase 2

Evaluating Low-dose Deferasirox (DFX) in Patients With Low-risk MDS Resistant or Relapsing After ESA Agents

Completed
NCT01892644Phase 2

Treatment of Iron Overload With Deferasirox (Exjade) in Hereditary Hemochromatosis and Myelodysplastic Syndrome

Withdrawn
NCT00749515Phase 4

Pilot Study for Patients With Poor Response to Deferasirox

Completed
NCT00419770Phase 2

The Deferasirox-AmBisome Therapy for Mucormycosis (DEFEAT Mucor) Study

Completed
NCT03920657Phase 2

Early and Low Dose Deferasirox (3.5 mg/kg FCT) to Suppress NTBI and LPI as Early Intervention to Prevent Tissue Iron Overload in Lower Risk MDS

Terminated
NCT00110266Phase 2

Study of Deferasirox for Treatment of Transfusional Iron Overload in Myelodysplastic Patients

Completed
NCT00845871Phase 4

Palatability and Tolerability of Deferasirox Taken With Meals, With Different Liquids or Crushed and Added to Food

Completed
NCT00117507Phase 4

Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients

Completed
NCT00447694Phase 2

Cardiac T2* in Beta-thalassemia Patients on Deferasirox Treatment

Completed
NCT01927913Phase 2

Treatment of Iron Overload Requiring Chelation Therapy

Withdrawn
NCT01825512Phase 3

Efficacy/Safety Study of Deferiprone Compared to Deferasirox in Paediatric Patients

Completed
NCT00560820Phase 1

Phase I Study to Examine the Effect of Deferasirox on Renal Hemodynamics in β-thalassemia Patients With Transfusional Iron Overload

Completed
NCT00432627Phase 1

Impact of Hepatic Impairment on the Pharmacokinetics of Deferasirox.

Completed
NCT00940602Phase 2

Myelodysplastic Syndromes (MDS) Event Free Survival With Iron Chelation Therapy Study

Completed
NCT03372083Phase 4

Safety Study of Crushed Deferasirox Film Coated Tablets in Pediatric Patients With Transfusional Hemosiderosis

Completed
NCT02943668Phase 2

Deferasirox in Treating Patients With Very Low, Low, or Intermediate-Risk Red Blood Cell Transfusion Dependent Anemia or Myelodysplastic Syndrome

Terminated
NCT02720536Phase 3

Extended Evaluation of Deferasirox Film-coated Tablet (FCT) Formulation

Completed
NCT02341495Phase 2

Deferasirox, Cholecalciferol, and Azacitidine in the Treatment of Newly Diagnosed AML Patients Over 65

Terminated

Drug Details

Intervention Type
DRUG
Total Trials
61