Success Metrics

Clinical Success Rate
92.3%

Based on 12 completed trials

Completion Rate
92%(12/13)
Active Trials
1(5%)
Results Posted
58%(7 trials)
Terminated
1(5%)

Phase Distribution

Ph not_applicable
3
14%
Ph phase_2
2
9%
Ph phase_4
8
36%
Ph phase_3
6
27%
Ph phase_1
1
5%

Phase Distribution

1

Early Stage

2

Mid Stage

14

Late Stage

Phase Distribution20 total trials
Phase 1Safety & dosage
1(5.0%)
Phase 2Efficacy & side effects
2(10.0%)
Phase 3Large-scale testing
6(30.0%)
Phase 4Post-market surveillance
8(40.0%)
N/ANon-phased studies
3(15.0%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

75.0%

12 of 16 finished

Non-Completion Rate

25.0%

4 ended early

Currently Active

1

trials recruiting

Total Trials

22

all time

Status Distribution
Active(2)
Completed(12)
Terminated(4)
Other(4)

Detailed Status

Completed12
unknown4
Withdrawn3
Enrolling by invitation1
Recruiting1
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
22
Active
1
Success Rate
92.3%
Most Advanced
Phase 4

Trials by Phase

Phase 11 (5.0%)
Phase 22 (10.0%)
Phase 36 (30.0%)
Phase 48 (40.0%)
N/A3 (15.0%)

Trials by Status

withdrawn314%
enrolling_by_invitation15%
completed1255%
recruiting15%
terminated15%
unknown418%

Recent Activity

Clinical Trials (22)

Showing 20 of 22 trialsScroll for more
NCT01999361Not Applicable

Prevention of de Novo Allosensitization in Islet Transplant Recipients Following Complete Graft Loss

Recruiting
NCT02081755Phase 4

Safety and Efficacy of Everolimus Treatment in Liver Transplantation for Liver Cancer

Enrolling By Invitation
NCT04645589

Evaluating the Safety of Myfortic (Mycophenolate Sodium) in Patients With Lupus Nephritis

Completed
NCT02130817Phase 4

Belatacept in Kidney Transplantation of Moderately Sensitized Patients

Withdrawn
NCT01092533Phase 3

Myfortic for the Treatment of Non-infectious Intermediate Uveitis

Completed
NCT00336817Not Applicable

A Prospective Study on the Tolerability and Efficacy of the de Novo Use of Myfortic in Liver Transplant Recipients

Completed
NCT00514514Phase 3

Study Investigating a Standard Regimen in de Novo Kidney Transplant Patients Versus a Calcineurin Inhibitor (CNI)-Free Regimen and a CNI-low Dose Regimen

Completed
NCT02058875Phase 4

Cardiovascular Risk Following Conversion to Full Dose Myfortic® and Neoral® Two-hour Post Level Monitoring

Withdrawn
NCT00336895Not Applicable

Conversion of CellCept to Myfortic: A Prospective Study in Liver Transplant Recipients

Completed
NCT00585468Phase 4

Pharmacokinetic Profile of Myfortic in Combination With Tacrolimus in Fed Versus Fasting State

Completed
NCT00652834Phase 4

Small Bowel Capsule Endoscopy Findings in Patients Receiving Cellcept®

Completed
NCT01018914Phase 4

A Study to Compare Safety and Efficacy of Prograf + Myfortic and Advagraf + Myfortic in Liver Transplantation Patients

Completed
NCT00298324Phase 3

Myfortic - Treatment for Extensive cGvHD

Terminated
NCT01596062Phase 2

Pharmacodynamics, Efficacy and Safety of Basiliximab 40 or 80 mg in Combination With Ciclosporine Microemulsion or Everolimus, in Adult Low Risk de Novo Renal Transplant Recipients (IDEALE Study)

Completed
NCT01079143Phase 3

Progression of Renal Interstitial Fibrosis / Tubular Atrophy (IF/TA) According to Epithelial-mesenchymal Transition (EMT) and Immunosuppressive Regimen (Everolimus Based Versus CNI Based) in de Novo Renal Transplant Recipients

Completed
NCT00167492Phase 4

Enteric Coated Myfortic for Liver Transplant Recipients

Withdrawn
NCT00298883Phase 1

Desensitization of Renal Transplant Candidates

Completed
NCT00890253Phase 2

Safety Study of Calcineurin-Inhibitor-Free Immunosuppression After Liver Transplantation

Unknown
NCT00101738Phase 3

Freedom Study: Myfortic in Kidney Transplant Patients

Completed
NCT01261169

Mycophenolate Sodium (Myfortic®) in the Treatment of Corticosteroid-refractory Autoimmune Uveitis:Pilot Study

Unknown

Drug Details

Intervention Type
DRUG
Total Trials
22