activated recombinant human factor VII
Phase 2Completed 1 views this week 0 watching💤 Quiet
Interest: 35/100
35
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Congenital Bleeding Disorder
Conditions
Congenital Bleeding Disorder, Haemophilia A With Inhibitors, Haemophilia B With Inhibitors
Trial Timeline
Mar 1, 2004 → Nov 1, 2005
NCT ID
NCT00108758About activated recombinant human factor VII
activated recombinant human factor VII is a phase 2 stage product being developed by Novo Nordisk for Congenital Bleeding Disorder. The current trial status is completed. This product is registered under clinical trial identifier NCT00108758. Target conditions include Congenital Bleeding Disorder, Haemophilia A With Inhibitors, Haemophilia B With Inhibitors.
What happened to similar drugs?
5 of 20 similar drugs in Congenital Bleeding Disorder were approved
Approved (5) Terminated (0) Active (15)
Hype Score Breakdown
Clinical
12
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (17)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01312636 | Pre-clinical | Completed |
| NCT01285089 | Pre-clinical | Completed |
| NCT01220141 | Pre-clinical | Completed |
| NCT01234545 | Pre-clinical | Completed |
| NCT00853086 | Pre-clinical | Completed |
| NCT00323570 | Phase 3 | Withdrawn |
| NCT01562457 | Phase 1 | Completed |
| NCT00123591 | Phase 2 | Completed |
| NCT00124293 | Pre-clinical | Completed |
| NCT00154427 | Phase 2 | Terminated |
| NCT00104455 | Phase 1 | Completed |
| NCT00154492 | Phase 2 | Completed |
| NCT00108758 | Phase 2 | Completed |
| NCT01476423 | Pre-clinical | Completed |
| NCT00571584 | Approved | Completed |
| NCT00426803 | Phase 2 | Completed |
| NCT01561352 | Phase 2 | Completed |
Competing Products
20 competing products in Congenital Bleeding Disorder
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Tideglusib | AMO Pharma | Pre-clinical | 20 |
| Tideglusib + Placebo | AMO Pharma | Phase 2/3 | 28 |
| Tideglusib | AMO Pharma | Phase 2/3 | 35 |
| EDIT-101 | Editas Medicine | Phase 1/2 | 18 |
| Tildacerfont/Placebo | Spruce Biosciences | Phase 2 | 17 |
| SPR001 | Spruce Biosciences | Phase 2 | 25 |
| SPR001 | Spruce Biosciences | Phase 2 | 25 |
| Tildacerfont/Placebo | Spruce Biosciences | Phase 2 | 17 |
| Tildacerfont | Spruce Biosciences | Phase 2 | 17 |
| KW-3357 | Kyowa Kirin | Phase 1 | 29 |
| Pasireotide 0.6Mg Solution for Injection + Saline Solution | Novartis | Phase 2 | 27 |
| Sandostatine LP | Novartis | Phase 2 | 35 |
| mycophenolate mofetil | Roche | Phase 1 | 29 |
| turoctocog alfa + turoctocog alfa | Novo Nordisk | Phase 3 | 40 |
| catridecacog + recombinant factor XIII | Novo Nordisk | Phase 1 | 29 |
| turoctocog alfa pegol | Novo Nordisk | Phase 3 | 40 |
| recombinant factor XIII | Novo Nordisk | Pre-clinical | 26 |
| activated recombinant human factor VII, long acting + activated recombinant human factor VII, long acting | Novo Nordisk | Phase 1 | 29 |
| Advate® + turoctocog alfa | Novo Nordisk | Phase 1 | 29 |
| nonacog beta pegol | Novo Nordisk | Phase 3 | 40 |