Golimumab
ApprovedCompleted 0 watching 0 views this week๐ฅ Hot
85
Development Stage
โ
Pre-clinicalโ
Phase 1โ
Phase 2โ
Phase 35
ApprovedIndication / Disease
Ankylosing Spondylitis
Conditions
Ankylosing Spondylitis
Trial Timeline
Sep 3, 2012 โ Apr 30, 2015
NCT ID
NCT01668004About Golimumab
Golimumab is a approved stage product being developed by Merck for Ankylosing Spondylitis. The current trial status is completed. This product is registered under clinical trial identifier NCT01668004. Target conditions include Ankylosing Spondylitis.
Hype Score Breakdown
Clinical
30
Activity
20
Company
10
Novelty
10
Community
12
Clinical Trials (6)
| NCT ID | Phase | Status |
|---|---|---|
| NCT03270501 | Phase 3 | Completed |
| NCT03124121 | Approved | Completed |
| NCT02841176 | Pre-clinical | Terminated |
| NCT02318667 | Approved | Completed |
| NCT02092285 | Approved | Completed |
| NCT01668004 | Approved | Completed |
Competing Products
20 competing products in Ankylosing Spondylitis
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Infliximab | Celltrion | Phase 1 | 33 |
| Infliximab | Celltrion | Phase 1 | 33 |
| SUNPG1622 I dose + Placebo dose | Sun Pharmaceutical | Phase 2 | 52 |
| adalimumab | Eisai | Phase 3 | 77 |
| Ixekizumab + Placebo + Adalimumab | Eli Lilly | Phase 3 | 77 |
| Tramadol /acetaminophen + Diclofenac | Johnson & Johnson | Approved | 85 |
| Golimumab + Placebo | Johnson & Johnson | Phase 3 | 77 |
| Golimumab | Johnson & Johnson | Approved | 85 |
| SHR0302 + SHR0302 placebo | Jiangsu Hengrui Medicine | Phase 2/3 | 65 |
| placebo for risankizumab + risankizumab | AbbVie | Phase 2 | 52 |
| Adalimumab | AbbVie | Approved | 85 |
| Upadacitinib + Placebo | AbbVie | Phase 2 | 52 |
| Adalimumab | AbbVie | Pre-clinical | 23 |
| infliximab + Placebo | Merck | Phase 3 | 77 |
| Infliximab | Merck | Approved | 85 |
| Infliximab + Placebo + Naproxen | Merck | Phase 3 | 77 |
| Infliximab | Merck | Pre-clinical | 23 |
| Remicade | Merck | Approved | 85 |
| Remicade | Merck | Approved | 85 |
| Infliximab | Merck | Approved | 85 |