SPN-812

ApprovedCompleted
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80
Hype Score

Development Stage

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

Attention-Deficit/Hyperactivity Disorder (ADHD)

Conditions

Attention-Deficit/Hyperactivity Disorder (ADHD)

Trial Timeline

Jul 27, 2021 โ†’ Jul 26, 2023

About SPN-812

SPN-812 is a approved stage product being developed by Supernus Pharmaceuticals for Attention-Deficit/Hyperactivity Disorder (ADHD). The current trial status is completed. This product is registered under clinical trial identifier NCT04786990. Target conditions include Attention-Deficit/Hyperactivity Disorder (ADHD).

Hype Score Breakdown

Clinical
30
Activity
20
Company
5
Novelty
10
Community
12

Clinical Trials (4)

NCT IDPhaseStatus
NCT06185985ApprovedCompleted
NCT04786990ApprovedCompleted
NCT04143217Phase 3Completed
NCT02736656Phase 3Active

Competing Products

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

See all competitors
ProductCompanyStageHype Score
atomoxetineEli LillyApproved
85
AtomoxetineEli LillyApproved
85
AtomoxetineEli LillyApproved
85
AtomoxetineEli LillyApproved
85
ABT-089 + atomoxetine + placeboAbbViePhase 2
52
ABT-089 + PlaceboAbbViePhase 2
52
ABT-089AbbViePhase 2
52
ABT-089 + placeboAbbViePhase 2
52
MK0249 + Concerta (methylphenidate) + PlaceboMerckPhase 2
52
Dex-Methylphenidate hydrochloride Extended Release (Focalinยฎ XR) + PlaceboNovartisApproved
85
IR Viloxazine + PlaceboSupernus PharmaceuticalsPhase 1/2
36
SPN-812Supernus PharmaceuticalsApproved
80
100mg SPN-812 + PlaceboSupernus PharmaceuticalsApproved
80
SPN-812Supernus PharmaceuticalsPhase 3
72
Placebo + SPN-812Supernus PharmaceuticalsPhase 3
72
Placebo + 100mg SPN-812 + 200mg SPN-812 + 300mg SPN-812 + 400mg SPN-812Supernus PharmaceuticalsPhase 2
47
SPN-812Supernus PharmaceuticalsPhase 3
72
TD-9855 + TD-9855 + PlaceboTheravance BiopharmaPhase 2
47