Atomoxetine
ApprovedCompleted 0 watching 0 views this week🔥 Hot
85
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Attention-Deficit/Hyperactivity Disorder
Conditions
Attention-Deficit/Hyperactivity Disorder
Trial Timeline
Apr 1, 2005 → Jun 1, 2006
NCT ID
NCT00191633About Atomoxetine
Atomoxetine is a approved stage product being developed by Eli Lilly for Attention-Deficit/Hyperactivity Disorder. The current trial status is completed. This product is registered under clinical trial identifier NCT00191633. Target conditions include Attention-Deficit/Hyperactivity Disorder.
Hype Score Breakdown
Clinical
30
Activity
20
Company
10
Novelty
10
Community
12
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01177943 | Phase 1 | Completed |
| NCT00969618 | Phase 3 | Completed |
| NCT00760747 | Approved | Completed |
| NCT00687609 | Approved | Terminated |
| NCT00636818 | Phase 2 | Completed |
| NCT00530335 | Phase 2 | Completed |
| NCT00471354 | Approved | Completed |
| NCT00918567 | Approved | Completed |
| NCT00299234 | Approved | Terminated |
| NCT00320528 | Phase 3 | Completed |
| NCT00252278 | Approved | UNKNOWN |
| NCT00255138 | Phase 3 | Withdrawn |
| NCT00953862 | Pre-clinical | Completed |
| NCT00191633 | Approved | Completed |
| NCT00286949 | Pre-clinical | Completed |
| NCT00488163 | Approved | Completed |
| NCT00191737 | Phase 3 | Completed |
| NCT00191516 | Phase 3 | Completed |
| NCT00191880 | Phase 3 | Completed |
| NCT00191035 | Approved | Completed |
Competing Products
18 competing products in Attention-Deficit/Hyperactivity Disorder
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| atomoxetine | Eli Lilly | Approved | 85 |
| Atomoxetine | Eli Lilly | Approved | 85 |
| Atomoxetine | Eli Lilly | Approved | 85 |
| ABT-089 + atomoxetine + placebo | AbbVie | Phase 2 | 52 |
| ABT-089 + Placebo | AbbVie | Phase 2 | 52 |
| ABT-089 | AbbVie | Phase 2 | 52 |
| ABT-089 + placebo | AbbVie | Phase 2 | 52 |
| MK0249 + Concerta (methylphenidate) + Placebo | Merck | Phase 2 | 52 |
| Dex-Methylphenidate hydrochloride Extended Release (Focalin® XR) + Placebo | Novartis | Approved | 85 |
| SPN-812 | Supernus Pharmaceuticals | Approved | 80 |
| IR Viloxazine + Placebo | Supernus Pharmaceuticals | Phase 1/2 | 36 |
| SPN-812 | Supernus Pharmaceuticals | Approved | 80 |
| 100mg SPN-812 + Placebo | Supernus Pharmaceuticals | Approved | 80 |
| SPN-812 | Supernus Pharmaceuticals | Phase 3 | 72 |
| Placebo + SPN-812 | Supernus Pharmaceuticals | Phase 3 | 72 |
| Placebo + 100mg SPN-812 + 200mg SPN-812 + 300mg SPN-812 + 400mg SPN-812 | Supernus Pharmaceuticals | Phase 2 | 47 |
| SPN-812 | Supernus Pharmaceuticals | Phase 3 | 72 |
| TD-9855 + TD-9855 + Placebo | Theravance Biopharma | Phase 2 | 47 |