Beriplex® P/N (Kcentra) + Fresh frozen plasma
Phase 3Completed 0 views this week 0 watching⚡ Active
Interest: 40/100
40
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Blood Coagulation Disorders
Conditions
Blood Coagulation Disorders, Acute Major Bleeding
Trial Timeline
Jun 1, 2008 → Nov 1, 2010
NCT ID
NCT00708435About Beriplex® P/N (Kcentra) + Fresh frozen plasma
Beriplex® P/N (Kcentra) + Fresh frozen plasma is a phase 3 stage product being developed by CSL for Blood Coagulation Disorders. The current trial status is completed. This product is registered under clinical trial identifier NCT00708435. Target conditions include Blood Coagulation Disorders, Acute Major Bleeding.
What happened to similar drugs?
7 of 16 similar drugs in Blood Coagulation Disorders were approved
Approved (7) Terminated (6) Active (6)
Hype Score Breakdown
Clinical
17
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (2)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00803101 | Phase 3 | Completed |
| NCT00708435 | Phase 3 | Completed |
Competing Products
20 competing products in Blood Coagulation Disorders
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| micafungin + voriconazole | Astellas Pharma | Approved | 35 |
| Cefiderocol | Shionogi | Phase 2 | 35 |
| Bunazosin + Doxazosin + Valsartin | Eisai | Approved | 43 |
| Pegfilgrastim | Kyowa Kirin | Phase 2 | 35 |
| epoetin alfa | Johnson & Johnson | Phase 2/3 | 38 |
| epoetin alfa | Johnson & Johnson | Phase 2/3 | 38 |
| epoetin alfa | Johnson & Johnson | Phase 2 | 35 |
| Metoprolol Succinate + Hydrochlorothiazide | AstraZeneca | Phase 3 | 40 |
| AZD6140 + Placebo | AstraZeneca | Phase 1 | 29 |
| NKTR-118 + moxifloxacin + Placebo | AstraZeneca | Phase 1 | 29 |
| MEDI-551 | AstraZeneca | Phase 1 | 29 |
| Ecallantide + Cyklokapron(R) | Merck | Phase 2 | 35 |
| Daptomycin | Merck | Phase 2 | 35 |
| ecallantide + placebo | Merck | Phase 2 | 35 |
| MK0859 | Merck | Phase 1 | 29 |
| Ecallantide + Placebo | Merck | Phase 2 | 27 |
| HSC835 | Novartis | Phase 2 | 35 |
| Aliskiren | Novartis | Approved | 35 |
| Aliskiren and HCTZ | Novartis | Approved | 43 |
| Aliskiren + Amlodipine + Placebo Aliskiren + Placebo Amlodipine | Novartis | Phase 2 | 35 |