CF101
Phase 3Completed 0 watching 0 views this week📈 Rising
69
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Keratoconjunctivitis Sicca
Conditions
Keratoconjunctivitis Sicca
Trial Timeline
Jul 1, 2011 → Dec 1, 2013
NCT ID
NCT01235234About CF101
CF101 is a phase 3 stage product being developed by Can Fite Biopharma for Keratoconjunctivitis Sicca. The current trial status is completed. This product is registered under clinical trial identifier NCT01235234. Target conditions include Keratoconjunctivitis Sicca.
Hype Score Breakdown
Clinical
27
Activity
18
Company
2
Novelty
9
Community
10
Clinical Trials (2)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01235234 | Phase 3 | Completed |
| NCT00280917 | Phase 2 | Completed |
Competing Products
15 competing products in Keratoconjunctivitis Sicca
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| FK506 | Astellas Pharma | Phase 3 | 77 |
| FK506 + placebo | Astellas Pharma | Phase 3 | 77 |
| OTX-101 0.09% | Sun Pharmaceutical | Phase 3 | 77 |
| OTX-101 0.05% + OTX-101 0.09% + Vehicle | Sun Pharmaceutical | Phase 2/3 | 65 |
| cyclosporine + vehicle of OTX-101 | Sun Pharmaceutical | Phase 3 | 77 |
| INS365 Ophthalmic Solution | Merck | Phase 3 | 77 |
| Pimecrolimus + Vehicle | Novartis | Phase 2 | 52 |
| Cyclosporine A + Dexamethasone | Novartis | Approved | 85 |
| Rebamipide | Novartis | Phase 3 | 77 |
| Rebamipide | Novartis | Phase 3 | 77 |
| Tasocitinib + Tasocitinib + vehicle for Tasocitinib | Pfizer | Phase 2 | 51 |
| Dupilumab | Regeneron Pharmaceuticals | Phase 2 | 51 |
| R348 Ophthalmic Solution, 0.2% + R348 Ophthalmic Solution, 0.5% + R348 Ophthalmic Solution, 1.0% + Placebo | Rigel Pharmaceuticals | Phase 1 | 25 |
| R348 Ophthalmic Solution, 0.2% + R348 Ophthalmic Solution, 0.5% + Placebo | Rigel Pharmaceuticals | Phase 2 | 44 |
| CF101 + Placebo | Can Fite Biopharma | Phase 2 | 44 |