Rivaroxaban (Xarelto,Bay 59-7939) + Acetylsalicylic acid(ASA)
Pre-clinicalCompletedDevelopment Stage
Prevention of Atherothrombotic Events
Prevention of Atherothrombotic Events, Coronary Artery Disease (CAD), Symptomatic Peripheral Artery Disease (Symptomatic PAD)
Feb 25, 2022 → Jun 6, 2024
About Rivaroxaban (Xarelto,Bay 59-7939) + Acetylsalicylic acid(ASA)
Rivaroxaban (Xarelto,Bay 59-7939) + Acetylsalicylic acid(ASA) is a pre-clinical stage product being developed by Bayer for Prevention of Atherothrombotic Events. The current trial status is completed. This product is registered under clinical trial identifier NCT04298567. Target conditions include Prevention of Atherothrombotic Events, Coronary Artery Disease (CAD), Symptomatic Peripheral Artery Disease (Symptomatic PAD).
What happened to similar drugs?
5 of 20 similar drugs in Prevention of Atherothrombotic Events were approved
Hype Score Breakdown
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT04298567 | Pre-clinical | Completed |
Competing Products
20 competing products in Prevention of Atherothrombotic Events
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| mRNA-1944 | Moderna | Phase 1 | 0 |
| Gam-COVID-Vac | Dr. Reddy's Laboratories | Phase 2/3 | 31 |
| edoxaban + enoxaparin sodium | Daiichi Sankyo | Phase 3 | 40 |
| Mifepristone | Eli Lilly | Phase 2 | 35 |
| EXANTA | AstraZeneca | Phase 2 | 27 |
| Risk of low dose aspirin discontinuation | AstraZeneca | Pre-clinical | 26 |
| DAPA/MET XR + DAPA + MET XR | AstraZeneca | Phase 3 | 40 |
| Esomeprazole + Placebo | AstraZeneca | Phase 3 | 40 |
| PCV15 | Merck | Pre-clinical | 18 |
| Raltegravir | Merck | Approved | 43 |
| RotaTeq (V260) + IPV | Merck | Phase 3 | 40 |
| V501 | Merck | Phase 3 | 40 |
| Zostavax | Merck | Phase 3 | 40 |
| V920 Consistency Lot A + V920 Consistency Lot B + V920 Consistency Lot C + V920 High-dose Lot + Placebo to V920 | Merck | Phase 3 | 40 |
| Letermovir + Placebo | Merck | Phase 3 | 40 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 43 |
| Enteric-coated mycophenolate sodium | Novartis | Phase 3 | 40 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 43 |
| rMenB+OMV NZ | Novartis | Phase 3 | 40 |
| Enteric-Coated Mycophenolate Sodium | Novartis | Phase 3 | 40 |