Ambrisentan
ApprovedCompleted 1 views this week 0 watching⚡ Active
Interest: 43/100
43
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Systemic Sclerosis
Conditions
Systemic Sclerosis, Shortness of Breath, Pulmonary Hypertension
Trial Timeline
Mar 1, 2009 → Jan 1, 2011
NCT ID
NCT01051960About Ambrisentan
Ambrisentan is a approved stage product being developed by Gilead Sciences for Systemic Sclerosis. The current trial status is completed. This product is registered under clinical trial identifier NCT01051960. Target conditions include Systemic Sclerosis, Shortness of Breath, Pulmonary Hypertension.
What happened to similar drugs?
9 of 20 similar drugs in Systemic Sclerosis were approved
Approved (9) Terminated (4) Active (8)
Hype Score Breakdown
Clinical
20
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (15)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01224210 | Phase 3 | Completed |
| NCT01072669 | Pre-clinical | Completed |
| NCT01093885 | Pre-clinical | Completed |
| NCT01051960 | Approved | Completed |
| NCT00840463 | Approved | Terminated |
| NCT00777920 | Phase 3 | Completed |
| NCT00851929 | Phase 2/3 | Completed |
| NCT01338636 | Approved | Completed |
| NCT00380068 | Phase 3 | Completed |
| NCT00423592 | Phase 2 | Completed |
| NCT00578786 | Phase 3 | Completed |
| NCT00091598 | Phase 3 | Completed |
| NCT00423202 | Phase 3 | Completed |
| NCT00423748 | Phase 3 | Completed |
| NCT00424021 | Phase 2 | Completed |
Competing Products
20 competing products in Systemic Sclerosis
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Tabalumab Auto-Injector + Tabalumab Prefilled Syringe | Eli Lilly | Phase 3 | 32 |
| Baricitinib + Placebo | Eli Lilly | Phase 2 | 35 |
| MRA(Tocilizumab) + placebo | Chugai Pharmaceutical | Phase 3 | 40 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 40 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 40 |
| DS-7011a + Placebo | Daiichi Sankyo | Phase 1 | 29 |
| DS-7011a + Placebo | Daiichi Sankyo | Phase 1/2 | 32 |
| Bocidelpar + Placebo | Astellas Pharma | Phase 1 | 21 |
| Parenteral micafungin application + Other parenteral antifungal drugs | Astellas Pharma | Pre-clinical | 26 |
| Micafungin | Astellas Pharma | Phase 2 | 35 |
| E6742 | Eisai | Phase 1/2 | 32 |
| KHK4827 | Kyowa Kirin | Phase 1 | 29 |
| KHK4827 + Placebo | Kyowa Kirin | Phase 3 | 40 |
| Baricitinib + Placebo | Eli Lilly | Phase 3 | 40 |
| Baricitinib + Cyclophosphamide | Eli Lilly | Approved | 47 |
| Baricitinib + Placebo | Eli Lilly | Phase 3 | 32 |
| LY2127399 + Placebo every 2 weeks + Placebo every 4 weeks + Standard of Care | Eli Lilly | Phase 3 | 40 |
| LY3361237 + Placebo | Eli Lilly | Phase 2 | 27 |
| LY2127399 + Placebo | Eli Lilly | Phase 3 | 32 |
| LY3361237 + Placebo | Eli Lilly | Phase 1 | 29 |