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
Arthroplasty, Replacement, Hip
Conditions
Arthroplasty, Replacement, Hip, Arthroplasty, Replacement, Knee
Trial Timeline
Oct 1, 2011 โ Jul 1, 2014
NCT ID
NCT01444586About Rivaroxaban (Xarelto, BAY59-7939)
Rivaroxaban (Xarelto, BAY59-7939) is a pre-clinical stage product being developed by Bayer for Arthroplasty, Replacement, Hip. The current trial status is completed. This product is registered under clinical trial identifier NCT01444586. Target conditions include Arthroplasty, Replacement, Hip, Arthroplasty, Replacement, Knee.
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| NCT01523418 | Pre-clinical | Withdrawn |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
9 competing products in Arthroplasty, Replacement, Hip
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| DU-176b | Daiichi Sankyo | Phase 2 | 52 |
| YM150 + Warfarin | Astellas Pharma | Phase 2 | 52 |
| Tapentadol IR (CG5503) + Placebo + Oxycodone HCL IR + Tapentadol IR (CG5503) | Johnson & Johnson | Phase 3 | 77 |
| Zoledronic acid 5mg | Novartis | Approved | 85 |
| Denosumab | Amgen | Phase 2 | 51 |
| JNJ-70033093 25 mg + JNJ-70033093 50 mg + JNJ-70033093 100 mg + JNJ-70033093 200 mg + Placebo + Enoxaparin 40 mg | Bristol Myers Squibb | Phase 2 | 51 |
| Enoxaparin sodium | Sanofi | Phase 3 | 76 |
| 48-hour ropivacaine infusions + Single dose ropivacaine + Patient controlled analgesics | Sanofi | Pre-clinical | 22 |
| Enoxaparin + Apixaban + BAY1213790 | Bayer | Phase 2 | 49 |