Biological
GLASSIA
GLASSIA is a biological therapy with 4 clinical trials. Historical success rate of 50.0%.
Total Trials
4
Max Phase
—
Type
BIOLOGICAL
Molecule
—
Success Metrics
Clinical Success Rate
50.0%
Based on 1 completed trials
Completion Rate
50%(1/2)
Active Trials
0(0%)
Results Posted
200%(2 trials)
Terminated
1(25%)
Phase Distribution
Ph phase_2
2
50%
Ph phase_3
1
25%
Phase Distribution
0
Early Stage
2
Mid Stage
1
Late Stage
Phase Distribution3 total trials
Phase 2Efficacy & side effects
2(66.7%)
Phase 3Large-scale testing
1(33.3%)
Highest Phase Reached
Phase 3Trial Status & Enrollment
Completion Rate
33.3%
1 of 3 finished
Non-Completion Rate
66.7%
2 ended early
Currently Active
0
trials recruiting
Total Trials
4
all time
Status Distribution
Completed(1)
Terminated(2)
Other(1)
Detailed Status
unknown1
Withdrawn1
Completed1
Terminated1
Development Timeline
Analytics
Development Status
Total Trials
4
Active
0
Success Rate
50.0%
Most Advanced
Phase 3
Trials by Phase
Phase 22 (66.7%)
Phase 31 (33.3%)
Trials by Status
unknown125%
withdrawn125%
completed125%
terminated125%
Recent Activity
0 active trials
Showing 4 of 4
completedphase_3
GLASSIA Safety, Immunogenicity, and Bronchoalveolar Lavage Study
NCT02525861
terminatedphase_2
A Phase 2/3 Study of GLASSIA for the Treatment of Acute GvHD
NCT02956122
unknown
Early Access Program Using Alpha 1 Antitrypsin Infusion for Patients With Steroid Refractory Acute GvHD After Hematopoietic Stem Cell Transplantation (HSCT)
NCT03172455
withdrawnphase_2
Study Comparing Weekly Intravenous Administration of OctaAlpha1 With a Marketed Preparation Glassia® in Subjects With Alpha-1-antitrypsin Deficiency
NCT03385395
Clinical Trials (4)
Showing 4 of 4 trials
NCT02525861Phase 3
GLASSIA Safety, Immunogenicity, and Bronchoalveolar Lavage Study
NCT02956122Phase 2
A Phase 2/3 Study of GLASSIA for the Treatment of Acute GvHD
NCT03172455
Early Access Program Using Alpha 1 Antitrypsin Infusion for Patients With Steroid Refractory Acute GvHD After Hematopoietic Stem Cell Transplantation (HSCT)
NCT03385395Phase 2
Study Comparing Weekly Intravenous Administration of OctaAlpha1 With a Marketed Preparation Glassia® in Subjects With Alpha-1-antitrypsin Deficiency
All 4 trials loaded
Drug Details
- Intervention Type
- BIOLOGICAL
- Total Trials
- 4