SUNPG1622 I dose + Placebo dose
Phase 2Terminated 0 watching 0 views this week⚡ Active
52
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Active Ankylosing Spondylitis or Non-Radiographic Axial Spondyloarthritis
Conditions
Active Ankylosing Spondylitis or Non-Radiographic Axial Spondyloarthritis
Trial Timeline
Nov 6, 2017 → Sep 3, 2019
NCT ID
NCT02980705About SUNPG1622 I dose + Placebo dose
SUNPG1622 I dose + Placebo dose is a phase 2 stage product being developed by Sun Pharmaceutical for Active Ankylosing Spondylitis or Non-Radiographic Axial Spondyloarthritis. The current trial status is terminated. This product is registered under clinical trial identifier NCT02980705. Target conditions include Active Ankylosing Spondylitis or Non-Radiographic Axial Spondyloarthritis.
Hype Score Breakdown
Clinical
17
Activity
12
Company
10
Novelty
5
Community
5
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT02980705 | Phase 2 | Terminated |
Competing Products
20 competing products in Active Ankylosing Spondylitis or Non-Radiographic Axial Spondyloarthritis
Other Products from Sun Pharmaceutical
Ilumya Injectable ProductApproved
85
CequaTM (Cyclosporine 0.09%) ophthalmic solutionApproved
85
Cyclosporine + Artificial tearApproved
85
AmifostineApproved
85
Ilaprazole antisecretory drug of each quadruple therapy the Ilaprazole -based quadruple therapy + Esoprazole antisecretory drug of each quadruple therapy Esoprazole-based quadruple therapyApproved
85