LCZ696
ApprovedCompleted 1 views this week 0 watching⚡ Active
Interest: 43/100
43
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Heart Failure With Reduced Ejection Fraction
Conditions
Heart Failure With Reduced Ejection Fraction
Trial Timeline
Feb 12, 2016 → Jun 20, 2018
NCT ID
NCT02661217About LCZ696
LCZ696 is a approved stage product being developed by Novartis for Heart Failure With Reduced Ejection Fraction. The current trial status is completed. This product is registered under clinical trial identifier NCT02661217. Target conditions include Heart Failure With Reduced Ejection Fraction.
What happened to similar drugs?
20 of 20 similar drugs in Heart Failure With Reduced Ejection Fraction were approved
Approved (20) Terminated (2) Active (0)
Hype Score Breakdown
Clinical
20
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (9)
| NCT ID | Phase | Status |
|---|---|---|
| NCT02389933 | Pre-clinical | Completed |
| NCT03909295 | Phase 3 | Terminated |
| NCT02661217 | Approved | Completed |
| NCT02226120 | Phase 3 | Completed |
| NCT01922089 | Phase 2 | Completed |
| NCT01621633 | Phase 2 | Completed |
| NCT01593787 | Phase 3 | Completed |
| NCT00913653 | Phase 2 | Completed |
| NCT01569815 | Phase 1 | Completed |
Competing Products
20 competing products in Heart Failure With Reduced Ejection Fraction
| 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 |