Sumitomo Pharma America
Sumitomo Pharma America sponsors 168 registered US clinical trials on ClinicalTrials.gov, 6 of them currently recruiting, and 142 completed. 83 of these trials are in Phase 3-4 (later-stage) and 80 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Schizophrenia, with 4 trials.
Trial Pipeline
168 total, page 3 of 4
A 6 Month Study of Once Daily Ciclesonide Hydrofluoroalkane (HFA) Nasal Aerosol in The Treatment of Perennial Allergic Rhinitis (PAR) in Subjects 12 Years and Older
NCT01067105
Study of the Effects of Ciclesonide Hydrofluoroalkane (HFA) Nasal Aerosol on Hypothalamic-Pituitary-Adrenal (HPA) Axis
NCT01033825
Clinical Trial to Assess the Efficacy and Safety of Ciclesonide Hydrofluoroalkane (HFA) Nasal Aerosol for the Treatment of Seasonal Allergic Rhinitis (SAR) to Mountain Cedar in Subjects 12 Years and Older
NCT01010971
Safety, Pharmacokinetics and Pharmacodynamics of DSP-8658 in Patients With Type 2 Diabetes Mellitus and Healthy Adults
NCT01042106
A 6 Month Safety and Efficacy Study of Once Daily Ciclesonide Hydrofluoroalkane (HFA) in the Treatment of Perennial Allergic Rhinitis (PAR) in Subjects 12 Years and Older
NCT00953147
Eslicarbazepine Acetate Monotherapy Long Term Study
NCT00910247
Safety Study of Arformoterol Tartrate Inhalation Solution in Chronic Obstructive Pulmonary Disease (COPD) Subjects
NCT00909779
Long Term Safety Study of Study Drug (Eszopiclone) in Children and Adolescents With ADHD -Associated Insomnia
NCT00857220
Effect of Calories and Fat Content on the Pharmacokinetics of Lurasidone HCl
NCT01074632
Safety & Efficacy Study of Study Drug (Eszopiclone) in Children and Adolescents With Attention-deficit/Hyperactivity Disorder - Associated Insomnia
NCT00856973
Lurasidone - A 6-week Study of Patients With Bipolar I Depression (Add-on)
NCT00868452
Safety and Efficacy of Eslicarbazepine Acetate Monotherapy in Subjects With Partial Epilepsy Not Well Controlled by Current Antiepileptic Drugs
NCT00866775
Lurasidone - A 6-week Study of Patients With Bipolar I Depression (Monotherapy)
NCT00868699
Lurasidone - A 24-week Extension Study of Patients With Bipolar I Depression
NCT00868959
A Study of BBI608 in Adult Patients With Advanced Malignancies
NCT01775423
Lurasidone HCl - A Long Term Phase 3 Study of Patients With Chronic Schizophrenia
NCT00789698
A Safety, Efficacy and Tolerability Study in Pediatric Subjects With Asthma
NCT00809757
Clinical Trial to Assess the Efficacy and Safety of Ciclesonide Hydrofluoroalkane (HFA) Nasal Aerosol for the Treatment of Seasonal Allergic Rhinitis
NCT00790023
Lurasidone HCL - A 6-week Phase 3 Study of Patients With Acute Schizophrenia.
NCT00790192
Midazolam Drug-Drug Interaction Study With Lurasidone HCl
NCT01082263
Digoxin Drug-Drug Interaction With Lurasidone HCl
NCT01082289
RI-AME Study OF [ISOTHIAZOLYL-3-14C]-LURASIDONE
NCT01082146
Rifampin Drug-Drug Interaction Study With Lurasidone HCl
NCT01082276
Lithium Drug-Drug Interaction Study With Lurasidone HCl
NCT01074073
The Bioequivalence Of Two Different Lurasidone Formulations In Patients
NCT01082250
Lurasidone HCl - A Long Term Safety Phase 3 Study of Patients With Clinically Stable Schizophrenia
NCT00641745
Lurasidone HCl A Phase 3 Study of Patients With Acute Schizophrenia
NCT00615433
Generalized Anxiety Disorder Proof of Concept Efficacy and Safety Study of SEP-225441 (Eszopiclone) In GAD Subjects
NCT00616655
A Safety and Tolerability Study of Arformoterol Tartrate Inhalation Solution in Pediatric Subjects
NCT00583947
A Safety, Efficacy and Tolerability Study of SEP-225289
NCT00584974
Efficacy Safety Study of Arformoterol QD Dosing Versus BID Dosing in COPD
NCT00571428
Lurasidone HCl: A Phase 3 Study of Patients With Acute Schizophrenia
NCT00549718
A Randomized, Placebo-Controlled, Two-Period, Crossover Study to Evaluate the Effect of Lurasidone HCl on Oral Contraceptive Pharmacokinetics in Healthy Female Subjects
NCT00549666
SMP-986 Phase 2 Proof of Concept in Patients With Overactive Bladder Syndrome (OABS)
NCT00409539
Efficacy Safety Study of Arformoterol/Tiotropium Combination Versus Either Therapy Alone in Chronic Obstructive Pulmonary Disease (COPD)
NCT00424528
A Long-Term Safety and Efficacy Study of Eszopiclone in Elderly With Primary Chronic Insomnia
NCT00386334
Safety and Efficacy Study of AC-3933 in Adults With Mild to Moderate Alzheimer's Disease
NCT00359944
Efficacy Study of Single-Dose Levalbuterol Tartrate HFA MDI Vs Placebo in Subjects 18 Years and Older With EIB
NCT00268723
Safety and Efficacy of Arformoterol Tartrate Inhalation Solution in Subjects With Chronic Obstructive Pulmonary Disease
NCT00250679
Reliability of a Top Mount Actuation Indicator With Levalbuterol MDI in Adult and Pediatric Subjects With Asthma or COPD
NCT00583986
Safety and Efficacy of Eszopiclone in Patients With Generalized Anxiety Disorder
NCT00235508
Study of Arformoterol Tartrate Inhalation Solution and Racemic Formoterol in Subjects With Mild to Moderate Chronic Obstructive Pulmonary Disease (COPD)
NCT00685529
A Study to Test the Safety and Tolerability of a New Medication in the Treatment of Schizophrenia
NCT00088621
A Study to Test the Effectiveness and Safety of a New Medication in the Treatment of Schizophrenia
NCT00088634
Study of Eszopiclone Compared to Placebo in the Treatment of Insomnia Secondary to Perimenopause/Menopause
NCT00366093
Study of Eszopiclone Compared to Placebo on Daytime Function in Subjects With Insomnia Related to Rheumatoid Arthritis
NCT00367965
A Study of Eszopiclone in Subjects With Insomnia Related to Major Depressive Disorder
NCT00368030
6-Month Chronic Efficacy & Safety Study of Eszopiclone in Adult Subjects With Primary Insomnia
NCT00352144
A Dose Ranging Study of Arformoterol Given Once Daily Compared to Arformoterol Given Twice Daily in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
NCT00691405
Safety and Efficacy of Eszopiclone With Mild to Moderate Obstructive Sleep Apnea Syndrome (OSAS)
NCT00685269
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 53 |
| Phase 2 | 27 |
| Phase 3 | 75 |
| Phase 4 | 8 |
Therapeutic Areas
What the Pipeline for Sumitomo Pharma America Shows
According to the ClinicalTrials.gov registry, Sumitomo Pharma America is linked to 168 US clinical trials across every stage of research activity. Of those, 6 studies are currently recruiting, about 4% of the sponsor's indexed portfolio, and 142 are already marked complete, representing roughly 85% of the total.
The phase mix for Sumitomo Pharma America reports 83 late-stage studies (Phase 3 and Phase 4 combined) and 80 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Sumitomo Pharma America is Schizophrenia with 4 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.