duloxetine hydrochloride + placebo
Phase 3Completed 0 views this week 0 watching⚡ Active
Interest: 40/100
40
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Anxiety Disorders
Conditions
Anxiety Disorders
Trial Timeline
Jun 1, 2004 → Sep 1, 2005
NCT ID
NCT00122824About duloxetine hydrochloride + placebo
duloxetine hydrochloride + placebo is a phase 3 stage product being developed by Eli Lilly for Anxiety Disorders. The current trial status is completed. This product is registered under clinical trial identifier NCT00122824. Target conditions include Anxiety Disorders.
What happened to similar drugs?
19 of 20 similar drugs in Anxiety Disorders were approved
Approved (19) Terminated (2) Active (1)
✅Usual dose treatment of Tandospirone + Comparative high dose of tandospirone treatmentSumitomo PharmaApproved
Hype Score Breakdown
Clinical
17
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (11)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00673452 | Approved | Completed |
| NCT00536471 | Approved | Completed |
| NCT00422162 | Approved | Completed |
| NCT00408993 | Phase 3 | Completed |
| NCT00406848 | Approved | Completed |
| NCT00244296 | Approved | Completed |
| NCT00191919 | Phase 3 | Completed |
| NCT00122863 | Phase 3 | Completed |
| NCT00122824 | Phase 3 | Completed |
| NCT00190996 | Phase 3 | Completed |
| NCT00058968 | Phase 3 | Completed |
Competing Products
20 competing products in Anxiety Disorders