Ranolazine + Placebo
Phase 3Terminated 0 views this week 0 watching💤 Quiet
Interest: 32/100
32
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Heart; Dysfunction Postoperative, Cardiac Surgery
Conditions
Heart; Dysfunction Postoperative, Cardiac Surgery
Trial Timeline
Sep 1, 2010 → Nov 1, 2012
NCT ID
NCT01352416About Ranolazine + Placebo
Ranolazine + Placebo is a phase 3 stage product being developed by Gilead Sciences for Heart; Dysfunction Postoperative, Cardiac Surgery. The current trial status is terminated. This product is registered under clinical trial identifier NCT01352416. Target conditions include Heart; Dysfunction Postoperative, Cardiac Surgery.
What happened to similar drugs?
20 of 20 similar drugs in Heart; Dysfunction Postoperative, Cardiac Surgery were approved
Approved (20) Terminated (2) Active (0)
Hype Score Breakdown
Clinical
17
Activity
0
Company
15
Novelty
0
Community
0
Clinical Trials (18)
| NCT ID | Phase | Status |
|---|---|---|
| NCT03044964 | Approved | UNKNOWN |
| NCT02829034 | Approved | Completed |
| NCT02423265 | Approved | Withdrawn |
| NCT02147067 | Phase 2 | Completed |
| NCT02156336 | Approved | Terminated |
| NCT02052011 | Approved | Completed |
| NCT01948310 | Approved | Completed |
| NCT01887353 | Phase 2 | Terminated |
| NCT01767987 | Phase 2 | Terminated |
| NCT01590979 | Pre-clinical | Terminated |
| NCT01558830 | Approved | UNKNOWN |
| NCT01472185 | Phase 3 | Completed |
| NCT01442038 | Phase 3 | Completed |
| NCT01505179 | Pre-clinical | Completed |
| NCT01352416 | Phase 3 | Terminated |
| NCT01163721 | Phase 2 | Completed |
| NCT00832572 | Approved | Terminated |
| NCT00099788 | Phase 3 | Completed |
Competing Products
20 competing products in Heart; Dysfunction Postoperative, Cardiac Surgery
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| mRNA-0184 | Moderna | Phase 1 | 0 |
| IV diuretic | Nuwellis | Pre-clinical | 16 |
| IV Loop Diuretics | Nuwellis | Pre-clinical | 23 |
| Stepped pharmacologic care | Nuwellis | Phase 3 | 30 |
| IV Loop Diuretics (LD) | Nuwellis | Pre-clinical | 8 |
| TRV120027 + Normal Saline | Trevena | Phase 1 | 19 |
| TRV027 Dose #1 + TRV027 Dose #2 + TRV027 Dose #3 + Placebo | Trevena | Phase 2 | 25 |
| TRV120027 + Placebo | Trevena | Phase 1/2 | 22 |
| Ilofotase alfa + Placebo | AM-Pharma | Phase 2 | 25 |
| INXN-4001 | Precigen | Phase 1 | 23 |
| LY3461767 + Placebo | Eli Lilly | Phase 1 | 29 |
| SGLT2i, beta blocker, ARNI, MRA, MTD | Eli Lilly | Approved | 43 |
| Pactimibe, CS-505 | Daiichi Sankyo | Phase 2 | 35 |
| Prasugrel 10 mg daily x 2 weeks + Clopidogrel 75 mg daily x 2 weeks | Daiichi Sankyo | Approved | 43 |
| olmesartan medoxomil + candesartan cilexetil placebo + olmesartan medoxomil placebo + candesartan cilexetil | Daiichi Sankyo | Phase 3 | 32 |
| Olmesartan | Daiichi Sankyo | Phase 3 | 40 |
| Carperitide + Placebo | Daiichi Sankyo | Phase 2 | 35 |
| Edoxaban | Daiichi Sankyo | Pre-clinical | 22 |
| Regadenoson | Astellas Pharma | Phase 1 | 29 |
| Advagraf + Prograf | Astellas Pharma | Phase 2 | 35 |