Osilodrostat
Pre-clinicalCompleted 0 watching 0 views this week๐ค Quiet
20
Development Stage
1
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Cushing's Syndrome
Conditions
Cushing's Syndrome
Trial Timeline
Jan 16, 2023 โ Oct 30, 2023
NCT ID
NCT05633953About Osilodrostat
Osilodrostat is a pre-clinical stage product being developed by Recordati for Cushing's Syndrome. The current trial status is completed. This product is registered under clinical trial identifier NCT05633953. Target conditions include Cushing's Syndrome.
Hype Score Breakdown
Clinical
5
Activity
2
Company
7
Novelty
2
Community
1
Clinical Trials (4)
| NCT ID | Phase | Status |
|---|---|---|
| NCT06430528 | Pre-clinical | Recruiting |
| NCT05633953 | Pre-clinical | Completed |
| NCT05382156 | Pre-clinical | Active |
| NCT03606408 | Phase 2 | Completed |
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 |
| 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 |
| Cushing's syndrome confirmation | Corcept Therapeutics | Pre-clinical | 18 |
| Mifepristone | Corcept Therapeutics | Phase 3 | 72 |
| mifepristone | Corcept Therapeutics | Phase 3 | 72 |
| mifepristone | Corcept Therapeutics | Phase 3 | 72 |