Success Metrics

Clinical Success Rate
76.0%

Based on 19 completed trials

Completion Rate
76%(19/25)
Active Trials
2(7%)
Results Posted
111%(21 trials)
Terminated
6(20%)

Phase Distribution

Ph phase_1
12
40%
Ph not_applicable
2
7%
Ph phase_2
9
30%
Ph phase_3
5
17%
Ph phase_4
1
3%

Phase Distribution

12

Early Stage

9

Mid Stage

6

Late Stage

Phase Distribution29 total trials
Phase 1Safety & dosage
12(41.4%)
Phase 2Efficacy & side effects
9(31.0%)
Phase 3Large-scale testing
5(17.2%)
Phase 4Post-market surveillance
1(3.4%)
N/ANon-phased studies
2(6.9%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

73.1%

19 of 26 finished

Non-Completion Rate

26.9%

7 ended early

Currently Active

2

trials recruiting

Total Trials

30

all time

Status Distribution
Active(2)
Completed(19)
Terminated(7)
Other(2)

Detailed Status

Completed19
Terminated6
unknown2
Recruiting1
Withdrawn1
Active, not recruiting1

Development Timeline

Analytics

Development Status

Total Trials
30
Active
2
Success Rate
76.0%
Most Advanced
Phase 4

Trials by Phase

Phase 112 (41.4%)
Phase 29 (31.0%)
Phase 35 (17.2%)
Phase 41 (3.4%)
N/A2 (6.9%)

Trials by Status

recruiting13%
withdrawn13%
active_not_recruiting13%
completed1963%
terminated620%
unknown27%

Recent Activity

Clinical Trials (30)

Showing 20 of 30 trialsScroll for more
NCT04323748Phase 1

Dose Dense Rituximab for High Risk Newly Diagnosed Acute Immune Thrombocytopenic Purpura

Recruiting
NCT03531736Phase 1

T Cell Depleted Allogeneic Hematopoietic Stem Cell Transplantation Conditioned With a Reduced Intensity Regimen in Patients With Hematologic Malignancies and Aplastic Anemia

Active Not Recruiting
NCT06790420

RITUXIMAB BS Intravenous Infusion 100mg・500mg [Pfizer] Post-marketing Database Study

Completed
NCT00572013Phase 1

Rituxan and BEAM With Autologous Peripheral Blood Progenitor Transplant for Indolent Lymphoma

Completed
NCT04680962Phase 3

MabionCD20® Compared to MabThera® and Rituxan® in Patients With Rheumatoid Arthritis

Withdrawn
NCT00074165Phase 2

Treating Patients With Recurrent PCNSL With Carboplatin/BBBD and Adding Rituxan To The Treatment Regimen

Terminated
NCT00496873Phase 2

Evaluation of the Safety and Efficacy of Nipent, Cytoxan, and Rituxan

Completed
NCT02240407Phase 1

Re-administration of Intramuscular AAV9 in Patients With Late-Onset Pompe Disease

Completed
NCT02149121Phase 3

PK Similarity Prospective Phase 3 Study in Patients With Rheumatoid Arthritis

Completed
NCT02260804Phase 3

To Compare Efficacy and Safety Between CT-P10 and Rituxan in Patients With Low Tumour Burden Follicular Lymphoma

Completed
NCT02282514Phase 1

Stem Cell Transplantation for Stiff Person Syndrome (SPS)

Terminated
NCT00566696Phase 2

Mismatched Family Member Donor Transplantation for Children and Young Adults With High Risk Hematological Malignancies

Completed
NCT02819726Phase 1

PK, PD, Safety, and Efficacy of SAIT101 Versus MabThera® Versus Rituxan® in Patients With Rheumatoid Arthritis

Completed
NCT02162771Phase 3

To Demonstrate Equivalence of Pharmacokinetics and Noninferiority of Efficacy for CT-P10 in Comparison With Rituxan

Completed
NCT02296775Phase 1

Comparative Pharmacokinetic, Pharmacodynamic, Safety and Efficacy Study of Three Anti-CD20 Monoclonal Antibodies in Patients With Moderate to Severe Rheumatoid Arthritis

Completed
NCT01526057Phase 2

A Pharmacokinetic/Pharmacodynamic Study Comparing PF-05280586 To Rituximab In Subjects With Active Rheumatoid Arthritis With An Inadequate Response To TNF Inhibitors (REFLECTIONS B328-01)

Completed
NCT00089284Phase 1

Phase I/II Trial of Redox Regulation in Patients With Relapsed or Refractory CD20+ NHL

Terminated
NCT00067002Phase 2

Randomized Double Cord Blood Transplant Study

Completed
NCT01702961Not Applicable

Rituxan + BEAM and Auto Stem Cell Transplant for High Risk Lymphoma or Hodgkin's Disease

Completed
NCT01178216Phase 1

Use of Immune Globulin Plus Rituximab for Desensitization in Highly HLA Sensitized Patients Awaiting Deceased Donor Kidney Transplantation

Completed

Drug Details

Intervention Type
DRUG
Total Trials
30