BiotechTube

Strattera (atomoxetine)

ApprovedCompleted
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85
Hype Score

Development Stage

✓
Pre-clinical
✓
Phase 1
✓
Phase 2
✓
Phase 3
5
Approved
Indication / Disease

ADHD NOS

Conditions

ADHD NOS

Trial Timeline

Dec 1, 2003 → Jul 1, 2008

NCT ID
NCT00181766

About Strattera (atomoxetine)

Strattera (atomoxetine) is a approved stage product being developed by Eli Lilly for ADHD NOS. The current trial status is completed. This product is registered under clinical trial identifier NCT00181766. Target conditions include ADHD NOS.

Hype Score Breakdown

Clinical
30
Activity
20
Company
10
Novelty
10
Community
12

Clinical Trials (1)

NCT IDPhaseStatus
NCT00181766ApprovedCompleted

Competing Products

20 competing products in ADHD NOS

See all competitors
ProductCompanyStageHype Score
atomoxetineEli LillyApproved
85
Atomoxetine + placeboEli LillyApproved
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Atomoxetine Hydrochloride + placeboEli LillyApproved
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atomoxetine (Strattera)Eli LillyApproved
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Atomoxetine + stimulants (any approved ADHD medication)Eli LillyPre-clinical
23
dasotraline + PlaceboSumitomo PharmaPhase 3
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dasotralineSumitomo PharmaPhase 1
33
dasotraline 4mgSumitomo PharmaPhase 3
77
AZD1446 + AZD1446 + AZD1446 + PlaceboAstraZenecaPhase 2
52
Placebo + AZD3480 + AZD3480AstraZenecaPhase 2
52
MK0249 + Concerta (methylphenidate) + PlaceboMerckPhase 2
52
Focalin XRNovartisPhase 3
77
Dex-Methylphenidate hydrochloride Extended Release (Focalin® XR) + PlaceboNovartisApproved
85
Dexmethylphenidate HCl extended-release capsulesNovartisPhase 3
77
Methylphenidate hydrochlorideNovartisPhase 3
77
Focalin XRNovartisPhase 3
77
methylphenidate HCl ERCT + PlaceboPfizerApproved
84
methylphenidate HCl ERCTPfizerApproved
84
Very Low Dose Quillivant XR + Low Dose Quillivant XR + Moderate Dose Quillivant XRPfizerApproved
84
BrexpiprazoleLundbeckPhase 1
30

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