Search clinical trials for: Divalproex Sodium ER

Total 11099 results

Southern California University of Health Sciences
Sun Ten Pharmaceutical Co Ltd.

Completed

Effects of Lagenbone on Bone Mineral Density

Osteoporosis

United States
Trevi Therapeutics
Syneos Health

Unknown

Nalbuphine ER Effects of Liver Disease on Pharmacokinetics and Itch

Hepatic Impairment | Nalbuphine

United States
Abbott

Completed

An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treatment of Mania/Bipolar Disorder in Children and Adolescents

Bipolar Disorder

United States
Abbott

Terminated

A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatment of Partial Seizures in Children

Partial Seizure Disorder

United States
Virginia Commonwealth University
Abbott

Completed

Tolerability and Efficacy of Depakote-extended Release in the Elderly

Epilepsy | Seizures | Elderly

United States
Dr. Reddy's Laboratories Limited

Completed

Bioequivalence Study of Divalproex Sodium Capsules(Sprinkle),125 mg of Dr. Reddy's Under Fasting Condition (Apple Sauce)

Healthy

India
Kowa Company, Ltd.

Completed

A Phase III Confirmatory Study of K-877 Extended Release Tablet

Dyslipidemias

Japan
UConn Health

Completed

Vaccination Efficacy With Metformin in Older Adults (VEME)

Aging | Vaccine Response Impaired | Age-Related Immunodeficiency

United States
Bellus Health Inc. - a GSK company

Recruiting

Assessment of the Pharmacokinetics of BLU-5937 Extended Release Prototypes and a BLU-5937 Immediate Release Reference Formulation

Healthy | Cough

United Kingdom
Yuzuncu Yıl University

Completed

Evaluation of Dental Anxiety in Second-Stage Implant Surgery With Er,Cr:YSGG Laser

Dental Anxiety

Turkey
Hopital de l'Enfant-Jesus

Unknown

Immobilization After an Anterior Glenohumeral Joint Dislocation With a Bankart Lesion

Glenohumeral Joint Dislocation

Canada
Teva Pharmaceuticals USA

Completed

Divalproex Sodium 500 mg Extended Release Tablets Under Fasting Conditions

Healthy

United States
Zurich University of Applied Sciences

Completed

Sport Specific Adaptions in Female Volleyball Players

Overuse Related Shoulder Problems

Switzerland
AstraZeneca

Completed

PET Study in Parkinson's Disease Patients

Parkinson's Disease

Sweden
Virginia Commonwealth University
Puma Biotechnology, Inc.

Recruiting

Neratinib + Valproate in Advanced Solid Tumors, w/Expansion Cohort in Ras-Mutated Ca

Solid Tumor, Adult

United States
Queen Mary University of London
Rosetrees Trust; The Drummond Foundation; East Anglian Air Ambulance; The Dowager...

Not yet recruiting

Emergency Resuscitative Endovascular Balloon Occlusion of the Aorta in Out of Hospital Cardiac Arrest (ERICA-ARREST)

Ventricular Fibrillation | Cardiac Arrest | Ventricular Arrythmia | Cardiac Arrhythmia | Pulseless Electrical Activity | Out-Of-Hospital Cardiac Arrest
Yale University

Completed

Resuscitative EndoVascular Aortic Occlusion for Maximal Perfusion (REVAMP)

Cardiac Arrest

United States
City, University of London

Unknown

Testing a Novel Parenting Intervention for Children With Autism (PAREint)

Autism Spectrum Disorder

United Kingdom
Ultragenyx Pharmaceutical Inc

Completed

A Phase 2 Study to Evaluate the Dose and Pharmacodynamic Efficacy of Sialic Acid-Extended Release (SA-ER) Tablets in Patients With GNE Myopathy or Hereditary Inclusion Body Myopathy (GNE Myopathy)

Hereditary Inclusion Body Myopathy | GNE Myopathy

United States, Israel
Emalex Biosciences Inc.
Syneos Health; Nuventra

Completed

Drug-Drug Interaction Study to Evaluate the Effect of Inhibition of UGTs on the PK of Ecopipam and Its Active Metabolite

Drug Interaction

United States
Dana-Farber Cancer Institute

Completed

Eribulin in HER2 Negative Metastatic BrCa

Breast Cancer

United States
University of British Columbia
Children's & Women's Health Centre of British Columbia

Withdrawn

Sup-ER Splint for Children With Birth Related Brachial Plexus Injury

Birth Related Brachial Plexus Injury | Obstetrical Brachial Plexus Palsy
Ultragenyx Pharmaceutical Inc

Completed

Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Sialic Acid in Patients With Glucosamine (UDP-N-acetyl)-2-epimerase Myopathy (GNEM) or Hereditary Inclusion Body Myopathy (HIBM) (GNEM)

Hereditary Inclusion Body Myopathy | GNE Myopathy | Distal Myopathy With Rimmed Vacuoles | Distal Myopathy, Nonaka Type

United States, Canada, United Kingdom, Israel, Italy, Bulgaria, France
Seattle Institute for Biomedical and Clinical Research
Abbott

Completed

Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood and/or Anxiety Symptoms

Alcoholism | Mood Disorders | Alcohol Related Disorders

United States
Montefiore Medical Center

Not yet recruiting

Efficacy and Tolerability of a Fractional Ablative Erbium Laser for Axillary Scarring for Hidradenitis Suppurativa Patients

Hidradenitis Suppurativa | Scarring

United States
Sir Run Run Shaw Hospital

Unknown

Laparoscopy Combined With Enhanced Recovery Pathway

Crohn's Disease

China
Universidad de Valparaiso
Universidade Estadual de Ponta Grossa

Unknown

Clinical Trial of the Effect of Different Categories of Adhesive System

Dental Caries

Chile
Pfizer

Completed

BIOEQUIVALENCE STUDY IN HEALTHY PARTICIPANTS COMPARING 4 MG AND 8 MG FESOTERODINE EXTENDED-RELEASE TABLETS (TOVIAZ™), MANUFACTURED AT ZWICKAU VERSUS FREIBURG

Neurogenic Detrusor Overactivity

Belgium
University of Virginia

Terminated

Stereotactic Radiosurgery With Nivolumab and Valproate in Patients With Recurrent Glioblastoma

Glioblastoma

United States
MapLight Therapeutics

Recruiting

ML-004 in Adolescents and Adults With Autism Spectrum Disorders (ASD)

Autism Spectrum Disorder

United States, Australia, Canada
The University of Hong Kong

Completed

Chinese Medicine Therapy on Menopausal Symptoms

Menopause

China
Boehringer Ingelheim

Completed

Study to Compare the Pharmacokinetics of Dipyridamole in Three Different Asasantin Extended Release (ER) Formulations in Healthy Male and Female Volunteers

Healthy
Dr. Reddy's Laboratories Limited

Completed

Bioequivalency Study of Divalproex Sodium DR Tablets, 500 mg of Dr.Reddy's Under Fasting Conditions

Healthy

India
University of California, San Francisco

Terminated

A Case Management Intervention to Prevent ER Visits in HIV-infected Persons

HIV

United States
Colgate Palmolive

Completed

Maximal Use Study to Determine the Pharmacokinetics of L-arginine After Exaggerated Oral Use of COL101

Caries,Dental

United States
Trevi Therapeutics

Recruiting

Cough Reduction in IPF With Nalbuphine ER (CORAL)

Idiopathic Pulmonary Fibrosis

United Kingdom, Australia, Netherlands, Spain, Italy, Poland, Turkey, Chile, Canada, Germany
University Hospital, Bordeaux

Completed

Multi-disciplinary Prevention Program (4P-ED)

Stroke

France
University of Washington
National Cancer Institute (NCI)

Completed

Eribulin Mesylate in Treating Patients With Recurrent or Metastatic Salivary Gland Cancer

Recurrent Salivary Gland Cancer | Stage IVA Salivary Gland Cancer | Stage IVB Salivary Gland Cancer | Stage IVC Salivary Gland Cancer

United States
Taipei City Hospital
Chang Gung Memorial Hospital

Completed

Lamotrigine for Ketamine Dependence Trial

Addiction

Taiwan
University of Southern California
National Cancer Institute (NCI)

Completed

Eribulin Mesylate in Treating Patients With Advanced or Recurrent Cervical Cancer

Recurrent Cervical Cancer | Stage IVA Cervical Cancer | Stage IVB Cervical Cancer | Stage IIIA Cervical Cancer | Stage IIIB Cervical Cancer

United States
Memorial University of Newfoundland

Withdrawn

Teaching Medical Students How to Suture: Standard Simulation vs in Situ

Laceration | Sutured Laceration
Boehringer Ingelheim

Completed

Bioequivalence of Pramipexole Extended Release (PPX ER) 1.5mg x 1 Tablet Once Daily (q.d.) vs. PPX ER 0.375mg x 4 Tablets Under Fasted and Fed Conditions in Japanese Healthy Volunteers

Healthy

Japan
Korea University Anam Hospital

Recruiting

A Study to Evaluate the Impact of Pre-procedural Intracoronary Nicorandil Injection to PREVENT reductioN Of decREased TIMI FLOW in Patients Who Undergoing Percutaneous Coronary Intervention for the Coronary Artery Disease

Coronary Artery Disease | Percutaneous Coronary Intervention | No-Reflow Phenomenon

Korea, Republic of
University of Sulaimani

Completed

Lasers as an Alternative to Formocresol and Sodium Hypochlorite Medicaments in Pulpotomy Techniques

Pulp Disease, Dental | Pulp Mummification

Iraq
Johns Hopkins Bloomberg School of Public Health

Recruiting

Southwest Hub for American Indian Youth Suicide Prevention Research

Suicide | Depressive Symptoms | Substance Use | Mental Health | Surveillance

United States
AstraZeneca
Biocard

Completed

An Open-label, Randomized, Crossover Study of Comparative Pharmacokinetics and Bioequivalence of Dapagliflozin + Metformin, 10 mg + 1000 mg Versus the Combined Use of Forxiga™, 10 mg and Two Glucophage® Long, ER Tablets, 500 mg Co-administered to Healthy Volunteers Under Standard Fed Conditions

Diabetes Mellitus, Type 2

Russian Federation
Mylan Pharmaceuticals Inc

Completed

Fed Bioequivalence Study of Divalproex Sodium Delayed-Release Tablets, 500 mg

Healthy

United States
AstraZeneca
Parexel

Completed

A Single Oral Dose Study to Evaluate Four Different Formulations of AZD9977 and the Effect of Food in Healthy Male Subjects

Healthy Volunteers

United Kingdom
Alembic Pharmaceuticals Ltd.

Completed

Comparative Bioavailability Study of Lamotrigine ER Tablets USP 50 mg

Bioequivalence

Canada
Stanford University

Completed

Single Session Pain Psychology Treatment: Comparative Efficacy & Mechanisms

Chronic Low Back Pain

United States

Search clinical trials for: Divalproex Sodium ER

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