canakinumab
Phase 3Completed 0 watching 0 views this week๐ Rising
77
Development Stage
โ
Pre-clinicalโ
Phase 1โ
Phase 24
Phase 35
ApprovedIndication / Disease
Systemic Juvenile Idiopathic Arthritis
Conditions
Systemic Juvenile Idiopathic Arthritis, Hereditary Periodic Fevers
Trial Timeline
Nov 3, 2014 โ Aug 31, 2018
NCT ID
NCT02334748About canakinumab
canakinumab is a phase 3 stage product being developed by Novartis for Systemic Juvenile Idiopathic Arthritis. The current trial status is completed. This product is registered under clinical trial identifier NCT02334748. Target conditions include Systemic Juvenile Idiopathic Arthritis, Hereditary Periodic Fevers.
Hype Score Breakdown
Clinical
27
Activity
18
Company
10
Novelty
9
Community
10
Clinical Trials (19)
| NCT ID | Phase | Status |
|---|---|---|
| NCT04476706 | Pre-clinical | Completed |
| NCT04795466 | Phase 2 | Terminated |
| NCT04717635 | Phase 3 | Completed |
| NCT04239157 | Phase 2 | Recruiting |
| NCT02980263 | Phase 2 | Withdrawn |
| NCT02756650 | Phase 2 | Completed |
| NCT02396212 | Phase 3 | Completed |
| NCT02334748 | Phase 3 | Completed |
| NCT01303380 | Phase 2 | Completed |
| NCT01276522 | Phase 2 | Completed |
| NCT01148797 | Phase 2 | Completed |
| NCT01170936 | Phase 2 | Completed |
| NCT01088880 | Phase 2 | Completed |
| NCT00991146 | Phase 3 | Completed |
| NCT00891046 | Phase 3 | Completed |
| NCT00927810 | Phase 2 | Completed |
| NCT00770601 | Phase 3 | Terminated |
| NCT00554606 | Phase 2 | Completed |
| NCT00487708 | Phase 2 | Completed |
Competing Products
20 competing products in Systemic Juvenile Idiopathic Arthritis
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Tabalumab Auto-Injector + Tabalumab Prefilled Syringe | Eli Lilly | Phase 3 | 77 |
| Baricitinib + Placebo | Eli Lilly | Phase 2 | 52 |
| MRA(Tocilizumab) + placebo | Chugai Pharmaceutical | Phase 3 | 77 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 77 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 77 |
| DS-7011a + Placebo | Daiichi Sankyo | Phase 1 | 33 |
| DS-7011a + Placebo | Daiichi Sankyo | Phase 1/2 | 41 |
| Bocidelpar + Placebo | Astellas Pharma | Phase 1 | 33 |
| Parenteral micafungin application + Other parenteral antifungal drugs | Astellas Pharma | Pre-clinical | 23 |
| Micafungin | Astellas Pharma | Phase 2 | 52 |
| E6742 | Eisai | Phase 1/2 | 41 |
| KHK4827 | Kyowa Kirin | Phase 1 | 33 |
| KHK4827 + Placebo | Kyowa Kirin | Phase 3 | 77 |
| Baricitinib + Placebo | Eli Lilly | Phase 3 | 77 |
| Baricitinib + Cyclophosphamide | Eli Lilly | Approved | 85 |
| Baricitinib + Placebo | Eli Lilly | Phase 3 | 77 |
| LY2127399 + Placebo every 2 weeks + Placebo every 4 weeks + Standard of Care | Eli Lilly | Phase 3 | 77 |
| LY3361237 + Placebo | Eli Lilly | Phase 2 | 52 |
| LY2127399 + Placebo | Eli Lilly | Phase 3 | 77 |
| LY3361237 + Placebo | Eli Lilly | Phase 1 | 33 |