Quetiapine
ApprovedTerminated 0 views this week 0 watching💤 Quiet
Interest: 35/100
35
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Generalized Anxiety Disorder
Conditions
Generalized Anxiety Disorder, Comorbid Opiate Dependence in Remission, Status Post Methadone-Maintenance Treatment
Trial Timeline
Jan 1, 2008 → Aug 1, 2011
NCT ID
NCT00668265About Quetiapine
Quetiapine is a approved stage product being developed by AstraZeneca for Generalized Anxiety Disorder. The current trial status is terminated. This product is registered under clinical trial identifier NCT00668265. Target conditions include Generalized Anxiety Disorder, Comorbid Opiate Dependence in Remission, Status Post Methadone-Maintenance Treatment.
What happened to similar drugs?
5 of 20 similar drugs in Generalized Anxiety Disorder were approved
Approved (5) Terminated (2) Active (13)
Hype Score Breakdown
Clinical
20
Activity
0
Company
15
Novelty
0
Community
0
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 Generalized Anxiety Disorder
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| atomoxetine + placebo | Eli Lilly | Phase 2/3 | 38 |
| Satralizumab | Chugai Pharmaceutical | Phase 3 | 32 |
| Perampanel | Eisai | Pre-clinical | 26 |
| Perampanel + Placebo comparator | Eisai | Phase 3 | 40 |
| zonisamide | Eisai | Pre-clinical | 26 |
| Fycompa | Eisai | Pre-clinical | 26 |
| Fycompa | Eisai | Pre-clinical | 26 |
| Perampanel | Eisai | Phase 3 | 40 |
| Perampanel | Eisai | Pre-clinical | 26 |
| Cenobamate | Ono Pharmaceutical | Phase 3 | 47 |
| Duloxetine + Placebo | Eli Lilly | Phase 3 | 40 |
| Duloxetine + Placebo | Eli Lilly | Approved | 43 |
| Ixekizumab | Eli Lilly | Approved | 43 |
| eszopiclone + eszopiclone + Placebo | Sumitomo Pharma | Phase 2 | 35 |
| Usual dose treatment of Tandospirone + Comparative high dose of tandospirone treatment | Sumitomo Pharma | Approved | 43 |
| ABBV-932 + Placebo for ABBV-932 + Antidepressant Therapy (ADT) | AbbVie | Phase 2 | 42 |
| Cariprazine 0.75 mg/day + Cariprazine 1.5 mg/day + Cariprazine 3.0 mg/day | AbbVie | Phase 2 | 27 |
| ABBV-932 + Placebo | AbbVie | Phase 1 | 29 |
| Escitalopram | AbbVie | Approved | 43 |
| Adalimumab | AbbVie | Phase 3 | 40 |