Other
Part B:
Part B: is an intervention with 6 clinical trials. Historical success rate of 100.0%.
Total Trials
6
Max Phase
—
Type
OTHER
Molecule
—
Success Metrics
Clinical Success Rate
100.0%
Based on 6 completed trials
Completion Rate
100%(6/6)
Active Trials
0(0%)
Results Posted
17%(1 trials)
Phase Distribution
Ph not_applicable
1
17%
Ph phase_2
1
17%
Ph phase_1
4
67%
Phase Distribution
4
Early Stage
1
Mid Stage
0
Late Stage
Phase Distribution6 total trials
Phase 1Safety & dosage
4(66.7%)
Phase 2Efficacy & side effects
1(16.7%)
N/ANon-phased studies
1(16.7%)
Highest Phase Reached
Phase 2Trial Status & Enrollment
Completion Rate
100.0%
6 of 6 finished
Non-Completion Rate
0.0%
0 ended early
Currently Active
0
trials recruiting
Total Trials
6
all time
Status Distribution
Completed(6)
Detailed Status
Completed6
Development Timeline
Analytics
Development Status
Total Trials
6
Active
0
Success Rate
100.0%
Most Advanced
Phase 2
Trials by Phase
Phase 14 (66.7%)
Phase 21 (16.7%)
N/A1 (16.7%)
Trials by Status
completed6100%
Recent Activity
0 active trials
Showing 5 of 6
completedphase_1
Safety, Tolerability and Pharmacokinetics of an Anti-PD-1 Monoclonal Antibody in Subjects With Advanced Malignancies
NCT03474640
completednot_applicable
Effects of an 8-day Advanced Meditation, Samyama on Physical, Psychological and Spiritual Wellbeing ,and Associated Neural Mechanisms
NCT04366544
completedphase_1
Oral CDX-7108 in Healthy Adults and EPI Subjects
NCT05082051
completedphase_1
Surufatinib DDI With a PPI and a CYP3A Inducer
NCT04510649
completedphase_1
A Study to Assess the Safety, Tolerability and Pharmacokinetics of AZD0914
NCT01929629
Clinical Trials (6)
Showing 6 of 6 trials
NCT03474640Phase 1
Safety, Tolerability and Pharmacokinetics of an Anti-PD-1 Monoclonal Antibody in Subjects With Advanced Malignancies
NCT04366544Not Applicable
Effects of an 8-day Advanced Meditation, Samyama on Physical, Psychological and Spiritual Wellbeing ,and Associated Neural Mechanisms
NCT05082051Phase 1
Oral CDX-7108 in Healthy Adults and EPI Subjects
NCT04510649Phase 1
Surufatinib DDI With a PPI and a CYP3A Inducer
NCT01929629Phase 1
A Study to Assess the Safety, Tolerability and Pharmacokinetics of AZD0914
NCT00291928Phase 2
HuMax-CD20 in Active Rheumatoid Arthritis, Phase I/II
All 6 trials loaded
Drug Details
- Intervention Type
- OTHER
- Total Trials
- 6