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Attention Deficit Disorder With Hyperactivity

15
Pipeline Programs
14
Companies
20
Clinical Trials
1 recruiting
1
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
1
0
6
0
4
4
Early DiscoveryClinical DevelopmentMarket

On Market (1)

Approved therapies currently available

Eli Lilly and Company
STRATTERAApproved
atomoxetine hydrochloride
Eli Lilly and Company
oral2002
2M Part D

Competitive Landscape

13 companies ranked by most advanced pipeline stage

Prevail Therapeutics
4 programs
2
1
Atomoxetine HydrochloridePhase 4
atomoxetinePhase 3
atomoxetinePhase 3
Efficacy of Atomoxetine in the Neuropsychological Tests Among Children With ADHDN/A
Angeles Therapeutics
Angeles TherapeuticsCA - Los Angeles
2 programs
1
GuanfacinePhase 41 trial
Leveraging Mobile Health Technology to Optimize Early Stimulant Medication Treatment: A Feasibility N/A1 trial
Active Trials
NCT01990222Completed26Est. Oct 2018
NCT00429273Completed212Est. Jul 2011
Eli Lilly and Company
Eli Lilly and CompanyINDIANAPOLIS, IN
1 program
1
atomoxetinePHASE_31 trial
Active Trials
NCT00386581Completed105Est. Feb 2005
Coordination Pharmaceuticals
1 program
1
Immediate-release MethylphenidatePhase 41 trial
Active Trials
NCT02951754Recruiting600Est. Dec 2032
Noven Pharmaceuticals
4 programs
2
2
Methylphenidate Transdermal SystemPhase 31 trial
Methylphenidate Transdermal SystemPhase 31 trial
Methylphenidate Transdermal SystemPhase 21 trial
Methylphenidate Transdermal SystemPhase 21 trial
Active Trials
NCT00151970Completed128Est. Oct 2006
NCT00466791Completed93Est. May 2005
NCT00151957Completed450Est. Jun 2007
+1 more trials
Otsuka
OtsukaJapan - Tokushima
2 programs
1
1
CTN SRPhase 21 trial
CTN XRPhase 11 trial
Active Trials
NCT07253441Completed174Est. Dec 2024
NCT02547428Completed85Est. Jun 2016
Pfizer
PfizerNEW YORK, NY
1 program
1
AtomoxetinePhase 21 trial
Active Trials
NCT00174226Completed241Est. Jan 2006
Supernus Pharmaceuticals
1 program
1
SPN-810Phase 21 trial
Active Trials
NCT00626236Completed78Est. Sep 2009
NLS Pharmaceutics
NLS PharmaceuticsSwitzerland - Zurich
1 program
1
mazindolPhase 21 trial
Active Trials
NCT02808104Completed84Est. Mar 2017
Human BioSciences
Human BioSciencesWV - Martinsburg
2 programs
Genetic, Brain Structure, and Environmental Effects on ADHDN/A1 trial
transcranial electrical stimulationN/A
Active Trials
NCT01721720Completed1,091Est. Jul 2024
Genome & Company
Genome & CompanyKorea - Suwon
1 program
Genetic, Brain Structure, and Environmental Effects on ADHDN/A
FundaMental Pharma
FundaMental PharmaGermany - Heidelberg
1 program
transcranial electrical stimulationN/A1 trial
Active Trials
NCT06974136Completed45Est. May 2026
Takeda
TakedaTOKYO, Japan
1 program
SPD503PHASE_35 trials
Active Trials
NCT01500694Completed215Est. Sep 2015
NCT00919867Completed42Est. Jul 2009
NCT00901576Completed38Est. Jul 2009
+2 more trials

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
Angeles TherapeuticsGuanfacine
Coordination PharmaceuticalsImmediate-release Methylphenidate
TakedaSPD503
Noven PharmaceuticalsMethylphenidate Transdermal System
Noven PharmaceuticalsMethylphenidate Transdermal System
Eli Lilly and Companyatomoxetine
TakedaSPD503
NLS Pharmaceuticsmazindol
OtsukaCTN SR
Supernus PharmaceuticalsSPN-810
Noven PharmaceuticalsMethylphenidate Transdermal System
PfizerAtomoxetine
TakedaSPD503
Noven PharmaceuticalsMethylphenidate Transdermal System
OtsukaCTN XR

Showing 15 of 20 trials with date data

Clinical Trials (20)

Total enrollment: 4,302 patients across 20 trials

Single Versus Combination Medication Treatment for Children With Attention Deficit Hyperactivity Disorder

Start: Jan 2007Est. completion: Jul 2011212 patients
Phase 4Completed
NCT02951754Coordination PharmaceuticalsImmediate-release Methylphenidate

Methylphenidate in Adults With Attention Deficit/Hyperactivity Disorder

Start: Feb 2002Est. completion: Dec 2032600 patients
Phase 4Recruiting

Access to Extended Release Guanfacine HCl for Subjects Who Participated in Studies SPD503-315 or SPD503-316 in Europe

Start: Mar 2012Est. completion: Sep 2015215 patients
Phase 3Completed
NCT00151983Noven PharmaceuticalsMethylphenidate Transdermal System

Safety & Tolerability of MTS in Children Aged 6-12 Diagnosed With ADHD & Previously Treated With Extended-Release Methylphenidate Therapy

Start: Jun 2005Est. completion: Jul 2006175 patients
Phase 3Completed
NCT00151957Noven PharmaceuticalsMethylphenidate Transdermal System

Safety and Tolerability of SPD485 in Children Aged 6-12 Diagnosed With ADHD and Previously Participated in MTS Trials

Start: Oct 2004Est. completion: Jun 2007450 patients
Phase 3Completed

Efficacy, Tolerability, and Safety of Once-Daily Atomoxetine Hydrochloride Versus Placebo in Russian Children and Adolescents With Attention-Deficit/Hyperactivity Disorder

Start: Jul 2004Est. completion: Feb 2005105 patients
Phase 3Completed

Safety and Efficacy of SPD503 in Treating Attention-Deficit/Hyperactivity Disorder (ADHD) in Children Aged 6-17

Start: Jan 2003Est. completion: Aug 2003345 patients
Phase 3Completed

Mazindol Controlled Release in Adults With Attention Deficit Hyperactivity Disorder (ADHD)

Start: Aug 2016Est. completion: Mar 201784 patients
Phase 2Completed

Safety and Efficacy Study of Centanafadine Sustained-Release (CTN SR) in Adults With Attention-Deficit Hyperactivity Disorder (ADHD)

Start: Aug 2015Est. completion: Jun 201685 patients
Phase 2Completed

Phase 2a Study of Safety and Tolerability of SPN-810 in Children With ADHD and Persistent Serious Conduct Problems

Start: Oct 2008Est. completion: Sep 200978 patients
Phase 2Completed
NCT00151970Noven PharmaceuticalsMethylphenidate Transdermal System

Efficacy, Safety and Tolerability of SPD485 in Children Aged 6-12 Diagnosed With ADHD

Start: Jun 2005Est. completion: Oct 2006128 patients
Phase 2Completed

Treatment of Adult ADHD With Atomoxetine or Atomoxetine and Buspar

Start: Nov 2004Est. completion: Jan 2006241 patients
Phase 2Completed

Safety and Tolerability of SPD503 and Psychostimulants in Children and Adolescents Aged 6-17 With Attention-Deficit/Hyperactivity Disorder (ADHD)

Start: Aug 2004Est. completion: Dec 200475 patients
Phase 2Completed
NCT00466791Noven PharmaceuticalsMethylphenidate Transdermal System

Classroom Study to Assess Efficacy and Safety of MTS in Pediatric Patients Aged 6-12 With ADHD

Start: Aug 2004Est. completion: May 200593 patients
Phase 2Completed

A Trial to Characterize Differences in Blood Levels of Different Lots of Centanafadine QD XR and to Understand the Effect of Food on Blood Levels

Start: Aug 2024Est. completion: Dec 2024174 patients
Phase 1Completed

A Drug Interaction Study of SPD503 and Vyvanse Administered Alone and In Combination in Normal Healthy Volunteers

Start: Jun 2009Est. completion: Jul 200942 patients
Phase 1Completed

A Drug Interaction Study of SPD503 and Concerta Administered Alone and In Combination in Normal Healthy Volunteers

Start: May 2009Est. completion: Jul 200938 patients
Phase 1Completed
NCT06974136FundaMental Pharmatranscranial electrical stimulation

tES Modalities for the Treatment of ADHD

Start: Mar 2025Est. completion: May 202645 patients
N/ACompleted
NCT01990222Angeles TherapeuticsLeveraging Mobile Health Technology to Optimize Early Stimulant Medication Treatment: A Feasibility

Leveraging Mobile Health Technology to Optimize Early Stimulant Medication Treatment: A Feasibility Pilot

Start: Jan 2014Est. completion: Oct 201826 patients
N/ACompleted
NCT01721720Human BioSciencesGenetic, Brain Structure, and Environmental Effects on ADHD

Genetic, Brain Structure, and Environmental Effects on ADHD

Start: Nov 2012Est. completion: Jul 20241,091 patients
N/ACompleted

Phase Legend

Preclinical— Lab & animal studies
Phase 1— Safety & dosing
Phase 2— Efficacy testing
Phase 3— Large-scale trials
On Market— Approved & available

Key Insights

4 late-stage (Phase 3) programs, potential near-term approvals
1 actively recruiting trials targeting 4,302 patients
14 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.