OROS Methylphenidate
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Interest: 43/100
43
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Attention Deficit Disorder With Hyperactivity
Conditions
Attention Deficit Disorder With Hyperactivity
Trial Timeline
Mar 1, 2008 → Jun 1, 2008
NCT ID
NCT00758160About OROS Methylphenidate
OROS Methylphenidate is a approved stage product being developed by Johnson & Johnson for Attention Deficit Disorder With Hyperactivity. The current trial status is completed. This product is registered under clinical trial identifier NCT00758160. Target conditions include Attention Deficit Disorder With Hyperactivity.
What happened to similar drugs?
11 of 20 similar drugs in Attention Deficit Disorder With Hyperactivity were approved
Approved (11) Terminated (1) Active (9)
Hype Score Breakdown
Clinical
20
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00758160 | Approved | Completed |
Competing Products
20 competing products in Attention Deficit Disorder With Hyperactivity
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| atomoxetine | Eli Lilly | Approved | 39 |
| Atomoxetine + Placebo | Eli Lilly | Phase 2/3 | 38 |
| Atomoxetine | Eli Lilly | Approved | 35 |
| Atomoxetine Hydrochloride | Eli Lilly | Approved | 43 |
| Atomoxetine | Eli Lilly | Phase 3 | 40 |
| Atomoxetine | Eli Lilly | Approved | 43 |
| Atomoxetine hydrochloride + Placebo | Eli Lilly | Approved | 43 |
| CLONICEL (Clonidine HCl sustained release) | Shionogi | Phase 3 | 40 |
| Donepezil hydrochloride + Placebo | Eisai | Phase 3 | 40 |
| LY2216684 + Methylphenidate + Placebo (tablet) + Placebo (capsule) | Eli Lilly | Phase 2/3 | 38 |
| Atomoxetine + Placebo | Eli Lilly | Approved | 43 |
| Atomoxetine | Eli Lilly | Approved | 43 |
| Atomoxetine | Eli Lilly | Pre-clinical | 26 |
| Atomoxetine Hydrochloride | Eli Lilly | Approved | 43 |
| Atomoxetine hydrochloride | Eli Lilly | Phase 3 | 40 |
| Atomoxetine Hydrochloride + Placebo | Eli Lilly | Approved | 43 |
| atomoxetine | Eli Lilly | Phase 3 | 40 |
| atomoxetine 0.5 mg/kg/day + placebo + atomoxetine 1.2 mg/kg/day + atomoxetine 1.2-1.4 mg/kg/day | Eli Lilly | Phase 3 | 40 |
| Atomoxetine Hydrochloride | Eli Lilly | Approved | 43 |
| Atomoxetine Hydrochloride | Eli Lilly | Phase 3 | 40 |