Dex-Methylphenidate hydrochloride Extended Release (Focalin® XR) + Placebo

ApprovedCompleted

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Interest: 43/100

Hype Score

Development Stage

✓

Pre-clinical

✓

Phase 1

✓

Phase 2

✓

Phase 3

Approved

Indication / Disease

Attention-Deficit/Hyperactivity Disorder (ADHD)

Conditions

Attention-Deficit/Hyperactivity Disorder (ADHD)

Trial Timeline

Oct 1, 2008 → Dec 1, 2008

NCT ID

NCT00776009

About Dex-Methylphenidate hydrochloride Extended Release (Focalin® XR) + Placebo

Dex-Methylphenidate hydrochloride Extended Release (Focalin® XR) + Placebo is a approved stage product being developed by Novartis for Attention-Deficit/Hyperactivity Disorder (ADHD). The current trial status is completed. This product is registered under clinical trial identifier NCT00776009. Target conditions include Attention-Deficit/Hyperactivity Disorder (ADHD).

What happened to similar drugs?

7 of 10 similar drugs in Attention-Deficit/Hyperactivity Disorder (ADHD) were approved

Approved (7) Terminated (0) Active (3)

✅atomoxetineEli LillyApproved

✅AtomoxetineEli LillyApproved

✅SPN-812Supernus PharmaceuticalsApproved

✅100mg SPN-812 + PlaceboSupernus PharmaceuticalsApproved

Hype Score Breakdown

Clinical

Activity

Company

Novelty

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Clinical Trials (1)

NCT ID	Phase	Status	Start	Completion	Indication
NCT00776009	Approved	Completed	Oct 1, 2008	Dec 1, 2008	Attention-Deficit/Hyperactivity Disorder (ADHD)

Competing Products

18 competing products in Attention-Deficit/Hyperactivity Disorder (ADHD)

See all competitors

Product	Company	Stage	Hype Score
atomoxetine	Eli Lilly	Approved	39
Atomoxetine	Eli Lilly	Approved	43
Atomoxetine	Eli Lilly	Approved	43
Atomoxetine	Eli Lilly	Approved	43
ABT-089 + atomoxetine + placebo	AbbVie	Phase 2	35
ABT-089 + Placebo	AbbVie	Phase 2	35
ABT-089	AbbVie	Phase 2	35
ABT-089 + placebo	AbbVie	Phase 2	35
MK0249 + Concerta (methylphenidate) + Placebo	Merck	Phase 2	35
SPN-812	Supernus Pharmaceuticals	Approved	37
IR Viloxazine + Placebo	Supernus Pharmaceuticals	Phase 1/2	26
SPN-812	Supernus Pharmaceuticals	Approved	37
100mg SPN-812 + Placebo	Supernus Pharmaceuticals	Approved	44
SPN-812	Supernus Pharmaceuticals	Phase 3	34
Placebo + SPN-812	Supernus Pharmaceuticals	Phase 3	34
Placebo + 100mg SPN-812 + 200mg SPN-812 + 300mg SPN-812 + 400mg SPN-812	Supernus Pharmaceuticals	Phase 2	29
SPN-812	Supernus Pharmaceuticals	Phase 3	38
TD-9855 + TD-9855 + Placebo	Theravance Biopharma	Phase 2	29