BT524 (Part I) + BT524 (Part II)
Phase 3Completed 0 views this week 0 watching💤 Quiet
Interest: 37/100
37
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Congenital Afibrinogenemia
Conditions
Congenital Afibrinogenemia, Congenital Hypofibrinogenemia
Trial Timeline
Mar 1, 2013 → Nov 18, 2020
NCT ID
NCT02065882About BT524 (Part I) + BT524 (Part II)
BT524 (Part I) + BT524 (Part II) is a phase 3 stage product being developed by ICON plc. for Congenital Afibrinogenemia. The current trial status is completed. This product is registered under clinical trial identifier NCT02065882. Target conditions include Congenital Afibrinogenemia, Congenital Hypofibrinogenemia.
What happened to similar drugs?
5 of 20 similar drugs in Congenital Afibrinogenemia were approved
Approved (5) Terminated (0) Active (15)
Hype Score Breakdown
Clinical
17
Activity
8
Company
12
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT02065882 | Phase 3 | Completed |
Competing Products
20 competing products in Congenital Afibrinogenemia
| 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 |
| activated recombinant human factor VII | Novo Nordisk | Phase 2 | 35 |
| 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 |