Rivaroxaban (Xarelto, BAY59-7939)
Pre-clinicalCompleted 0 watching 0 views this week๐ค Quiet
20
Development Stage
1
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Non-valvular Atrial Fibrillation (NVAF)
Conditions
Non-valvular Atrial Fibrillation (NVAF)
Trial Timeline
May 13, 2020 โ Jan 16, 2023
NCT ID
NCT04356989About Rivaroxaban (Xarelto, BAY59-7939)
Rivaroxaban (Xarelto, BAY59-7939) is a pre-clinical stage product being developed by Bayer for Non-valvular Atrial Fibrillation (NVAF). The current trial status is completed. This product is registered under clinical trial identifier NCT04356989. Target conditions include Non-valvular Atrial Fibrillation (NVAF).
Hype Score Breakdown
Clinical
5
Activity
2
Company
7
Novelty
2
Community
1
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT06193863 | Pre-clinical | Active |
| NCT04923139 | Pre-clinical | Completed |
| NCT04356989 | Pre-clinical | Completed |
| NCT04174859 | Pre-clinical | Completed |
| NCT03455439 | Pre-clinical | Completed |
| NCT03284762 | Pre-clinical | Completed |
| NCT03214172 | Pre-clinical | Completed |
| NCT02975453 | Pre-clinical | Completed |
| NCT03242278 | Pre-clinical | Completed |
| NCT02564718 | Phase 1/2 | Completed |
| NCT02558465 | Pre-clinical | Completed |
| NCT02309411 | Phase 2 | Completed |
| NCT02262676 | Pre-clinical | Completed |
| NCT01523418 | Pre-clinical | Withdrawn |
| NCT01839357 | Phase 3 | Completed |
| NCT01855100 | Pre-clinical | Completed |
| NCT01855139 | Pre-clinical | Completed |
| NCT01853800 | Phase 1 | Completed |
| NCT01805544 | Pre-clinical | Completed |
| NCT01805531 | Pre-clinical | Completed |
Competing Products
17 competing products in Non-valvular Atrial Fibrillation (NVAF)
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Edoxaban | Daiichi Sankyo | Pre-clinical | 23 |
| DU-176b 15mg + DU-176b 30mg + DU-176b 60mg | Daiichi Sankyo | Phase 3 | 77 |
| Edoxaban + Aspirin and Clopidogrel + Aspirin and Warfarin | Daiichi Sankyo | Approved | 85 |
| Edoxaban | Daiichi Sankyo | Pre-clinical | 23 |
| AZD0837 + Aspirin | AstraZeneca | Phase 2 | 52 |
| Apixaban + Warfarin | Pfizer | Pre-clinical | 22 |
| Warfarin + Apixaban | Pfizer | Pre-clinical | 22 |
| Apixaban | Bristol Myers Squibb | Approved | 84 |
| Apixaban | Bristol Myers Squibb | Pre-clinical | 22 |
| Rivaroxaban(Xarelto,BAY 59-7939) | Bayer | Pre-clinical | 20 |
| Rivaroxaban (Xarelto,Bay 59-7939) | Bayer | Pre-clinical | 20 |
| Rivaroxaban (Xarelto, BAY59-7939) + Warfarin | Bayer | Pre-clinical | 20 |
| Rivaroxaban (Xarelto, BAY-597939) + VKAs | Bayer | Pre-clinical | 20 |
| Non-VKA Oral Anticoagulants (NOAC) | Bayer | Pre-clinical | 20 |
| Rivaroxaban (Xarelto, BAY59-7939) | Bayer | Pre-clinical | 20 |
| Rivaroxaban (Xarelto_ BAY59-7939) | Bayer | Pre-clinical | 20 |
| Rivaroxaban (Xarelto, BAY59-7939) + Apixaban (Eliquis) + Dabigatran etexilate (Pradaxa) + Warfarin (Marevan) | Bayer | Pre-clinical | 20 |