Quetiapine
Phase 2Terminated 0 watching 0 views this week⚡ Active
52
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Postpartum Depressive Disorder
Conditions
Postpartum Depressive Disorder
Trial Timeline
Aug 1, 2007 → Oct 1, 2008
NCT ID
NCT00681668About Quetiapine
Quetiapine is a phase 2 stage product being developed by AstraZeneca for Postpartum Depressive Disorder. The current trial status is terminated. This product is registered under clinical trial identifier NCT00681668. Target conditions include Postpartum Depressive Disorder.
Hype Score Breakdown
Clinical
17
Activity
12
Company
10
Novelty
5
Community
5
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01244711 | Approved | Terminated |
| NCT00554658 | Approved | Completed |
| NCT00668265 | Approved | Terminated |
| NCT01458964 | Approved | Completed |
| NCT00681668 | Phase 2 | Terminated |
| NCT00486798 | Phase 3 | Terminated |
| NCT00407199 | Approved | Completed |
| NCT00388973 | Phase 3 | Completed |
| NCT00302770 | Phase 3 | Terminated |
| NCT01224067 | Approved | Completed |
| NCT00232570 | Pre-clinical | UNKNOWN |
| NCT00232414 | Phase 3 | Completed |
| NCT00174603 | Phase 3 | Terminated |
| NCT00254813 | Phase 3 | Completed |
| NCT00252226 | Phase 3 | Completed |
| NCT00207064 | Pre-clinical | Completed |
| NCT00536783 | Pre-clinical | Completed |
| NCT00215254 | Phase 2/3 | Completed |
| NCT00156715 | Approved | Completed |
| NCT00277667 | Phase 3 | Completed |
Competing Products
20 competing products in Postpartum Depressive Disorder
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Misoprostol + Oxytocin | Cipla | Phase 3 | 77 |
| Azithromycin + Azithromycin and amoxicillin + Placebo | Merck | Approved | 85 |
| Eptacog alfa (NovoSeven) | Novo Nordisk | Approved | 84 |
| Eptacog alfa (activated) | Novo Nordisk | Pre-clinical | 22 |
| aripiprazole | Bristol Myers Squibb | Phase 3 | 76 |
| fibrinogen concentrate + Placebo | CSL | Phase 1/2 | 40 |
| SAGE-217 15/20 mg Oral Solution + Placebo + SAGE 217 30 mg Capsules | Biogen | Phase 3 | 74 |
| SAGE-217 + Placebo | Biogen | Phase 3 | 74 |
| Zuranolone | Biogen | Pre-clinical | 20 |
| Zuranolone | Biogen | Pre-clinical | 20 |
| LPCN 1154A + Placebo | Lipocine | Phase 3 | 69 |
| Goserelin 3.6 mg implant + Placebo | Brain Biotech | Pre-clinical | 15 |
| ZULRESSO (brexanolone) injection | Supernus Pharmaceuticals | Pre-clinical | 18 |
| Placebo + SAGE-547 90 μg/kg/h | Supernus Pharmaceuticals | Phase 3 | 72 |
| ZULRESSO® | Supernus Pharmaceuticals | Approved | 80 |
| SAGE-547 | Supernus Pharmaceuticals | Phase 2 | 47 |
| Placebo + SAGE-547 60 μg/kg/h + SAGE-547 90 μg/kg/h | Supernus Pharmaceuticals | Phase 3 | 72 |
| SAGE-547 + Placebo | Supernus Pharmaceuticals | Phase 2 | 47 |
| GH001 | GH Research | Phase 2 | 47 |
| Brexanolone | Brain Biotech | Pre-clinical | 15 |