Atomoxetine Hydrochloride + placebo
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Phase 35
ApprovedAbout Atomoxetine Hydrochloride + placebo
Atomoxetine Hydrochloride + placebo is a approved stage product being developed by Eli Lilly for ADHD. The current trial status is completed. This product is registered under clinical trial identifier NCT00190736. Target conditions include ADHD.
What happened to similar drugs?
9 of 20 similar drugs in ADHD were approved
Approved (9) Terminated (3) Active (10)
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Clinical Trials (12)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00700427 | Phase 3 | Completed |
| NCT00510276 | Approved | Completed |
| NCT00190879 | Approved | Completed |
| NCT00191945 | Phase 3 | Completed |
| NCT00191906 | Approved | Completed |
| NCT00190775 | Approved | Completed |
| NCT00190736 | Approved | Completed |
| NCT00485459 | Phase 3 | Completed |
| NCT00191698 | Phase 3 | Completed |
| NCT00190931 | Approved | Completed |
| NCT00191009 | Phase 2/3 | Completed |
| NCT00486122 | Approved | Completed |
Competing Products
20 competing products in ADHD