Success Metrics

Clinical Success Rate
86.2%

Based on 25 completed trials

Completion Rate
86%(25/29)
Active Trials
0(0%)
Results Posted
28%(7 trials)
Terminated
4(13%)

Phase Distribution

Ph phase_1
1
3%
Ph phase_3
10
31%
Ph phase_2
5
16%
Ph phase_4
13
41%
Ph not_applicable
2
6%

Phase Distribution

1

Early Stage

5

Mid Stage

23

Late Stage

Phase Distribution31 total trials
Phase 1Safety & dosage
1(3.2%)
Phase 2Efficacy & side effects
5(16.1%)
Phase 3Large-scale testing
10(32.3%)
Phase 4Post-market surveillance
13(41.9%)
N/ANon-phased studies
2(6.5%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

86.2%

25 of 29 finished

Non-Completion Rate

13.8%

4 ended early

Currently Active

0

trials recruiting

Total Trials

32

all time

Status Distribution
Completed(25)
Terminated(4)
Other(3)

Detailed Status

Completed25
Terminated4
unknown3

Development Timeline

Analytics

Development Status

Total Trials
32
Active
0
Success Rate
86.2%
Most Advanced
Phase 4

Trials by Phase

Phase 11 (3.2%)
Phase 25 (16.1%)
Phase 310 (32.3%)
Phase 413 (41.9%)
N/A2 (6.5%)

Trials by Status

terminated413%
unknown39%
completed2578%

Recent Activity

Clinical Trials (32)

Showing 20 of 32 trialsScroll for more
NCT02876211Phase 4

Paricalcitol Improves Anemia of Inflammation

Terminated
NCT00875004Not Applicable

Epoetin Beta in Patients Undergoing Chemotherapy for Solid Tumors

Terminated
NCT00717821Phase 3

A Study of Once Monthly Intravenous or Subcutaneous Mircera in Participants With Chronic Kidney Disease on Hemodialysis.

Completed
NCT02145026Phase 4

A Study of Epoetin Beta Treatment in Anemic Participants With Myelodysplastic Syndrome (MDS)

Completed
NCT00773513Phase 4

A Study to Assess All-Cause Mortality and Cardiovascular Morbidity in Participants With Chronic Kidney Disease (CKD) on Dialysis and Those Not on Renal Replacement Therapy Receiving Methoxy Polyethylene Glycol-Epoetin Beta (Mircera) or Reference Erythropoietin Stimulating Agents (ESAs)

Completed
NCT03658876Phase 4

Predictors of Response to Iron and Erythropoietin Stimulating Agents

Completed
NCT02761642Phase 2

A Study to Evaluate Efficacy and Safety of Epoetin Beta (NeoRecormon®) in Anemic Participants With Breast Cancer Undergoing Chemotherapy

Completed
NCT00776425Phase 4

A Study of the Quality of Life and Treatment Response to Once Weekly Epoetin Beta (Recormon) Treatment in Anemic Participants With Solid and Lymphoid Malignancies

Completed
NCT01718379Phase 2

Lenalidomide in Subject With Low and Intermediate-1 Risk MDS and Without Chromosome 5 Abnormality.

Completed
NCT02554942Phase 4

A Study of Epoetin Beta (NeoRecormon) in Participants With Solid Tumors

Completed
NCT02624141Phase 4

A Study of Recormon (Epoetin Beta) in Anemic Patients With Non-Myeloid Malignancy

Terminated
NCT02564094Phase 4

A Study of Epoetin Beta (NeoRecormon) in Participants With Solid Tumors or Hematologic Malignancies

Completed
NCT00773331Phase 3

A Study Comparing Maintenance of Hemoglobin Levels, Safety and Tolerability of Once Every 4 Weeks Mircera Versus Epoetin Beta in Dialysis Patients With Chronic Renal Anemia.

Completed
NCT00442793Phase 3

A Study Comparing Mircera and Epoetin Beta for the Treatment of Anemia in Dialysis Patients With Chronic Kidney Disease.

Completed
NCT02608060Phase 4

A Study to Assess the Hematopoyetic Response of Anemic Patients With Hematologic Malignancies Treated With Erythropoietin B

Terminated
NCT02569515Phase 4

A Study of Epoetin Beta (NeoRecormon) in Predialysis Patients With Renal Anemia

Completed
NCT01809314

An Observational Study of Epoetin Beta (NeoRecormon) in Participants With Cancer Receiving Chemotherapy

Completed
NCT02827266Phase 3

A Study of Epoetin Beta (NeoRecormon) in Anemic Participants With Diabetes and Chronic Renal Failure Who Are Not on Dialysis

Completed
NCT00354341Phase 3

(ACORD Study) - A Study of NeoRecormon (Epoetin Beta) in Patients With Early Diabetic Nephropathy

Completed
NCT01015352Phase 2

Azacitidine Combined to Epoetin Beta in International Prognostic Scoring System (IPSS) Low-risk and Intermediate-1 Myelodysplastic Syndrome (MDS) Patients, Resistant to Erythropoetin-stimulating Agents (ESA)

Completed

Drug Details

Intervention Type
DRUG
Total Trials
32