Cushing's syndrome confirmation
Pre-clinicalTerminated 0 watching 0 views this week๐ค Quiet
18
Development Stage
1
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Cushing's Syndrome
Conditions
Cushing's Syndrome
Trial Timeline
Feb 1, 2009 โ โ
NCT ID
NCT00796783About Cushing's syndrome confirmation
Cushing's syndrome confirmation is a pre-clinical stage product being developed by Corcept Therapeutics for Cushing's Syndrome. The current trial status is terminated. This product is registered under clinical trial identifier NCT00796783. Target conditions include Cushing's Syndrome.
Hype Score Breakdown
Clinical
5
Activity
2
Company
5
Novelty
2
Community
1
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00796783 | Pre-clinical | Terminated |
Competing Products
18 competing products in Cushing's Syndrome
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| AZD4017 and prednisolone + Placebo Oral Tablet and prednisolone | AstraZeneca | Phase 2 | 52 |
| pasireotide LAR + SOM230 LAR 30 mg + SOM230 LAR 10 mg | Novartis | Phase 3 | 77 |
| Pasireotide sub-cutaneous | Novartis | Phase 3 | 77 |
| osilodrostat + osilodrostat Placebo | Novartis | Phase 3 | 77 |
| Osilodrostat | Novartis | Phase 2 | 52 |
| Pasireotide | Novartis | Phase 3 | 77 |
| Pasireotide s.c. + Sitagliptin + Liraglutide + Insulin + Pasireotide LAR + Metformin | Novartis | Approved | 85 |
| SOM230 s.c. | Novartis | Phase 2 | 52 |
| Lu AG13909 | Lundbeck | Phase 2 | 49 |
| Osilodrostat | Recordati | Pre-clinical | 20 |
| Pasireotide + Cabergoline + Pasireotide LAR | Recordati | Approved | 82 |
| osilodrostat | Recordati | Phase 2 | 49 |
| Osilodrostat | Recordati | Pre-clinical | 20 |
| mifepristone | Corcept Therapeutics | Phase 3 | 72 |
| CORT125134 | Corcept Therapeutics | Phase 2 | 47 |
| Mifepristone | Corcept Therapeutics | Phase 3 | 72 |
| mifepristone | Corcept Therapeutics | Phase 3 | 72 |
| mifepristone | Corcept Therapeutics | Phase 3 | 72 |