Search clinical trials for: sodium zirconium cyclosilicate

Total 10172 results

Roswell Park Cancer Institute

Completed

Surgery and Photodynamic Therapy in Treating Patients With Malignant Mesothelioma

Malignant Mesothelioma

United States
Assistance Publique - Hôpitaux de Paris

Completed

PHARES Study: Management of Resistant Hypertension

Hypertension

France
Astellas Pharma Inc

Completed

A Study of the Effect of ASP1941 on Cardiac Repolarization in Healthy Subjects

Healthy Subjects | Cardiac Repolarization

United States
Consorci Sanitari de Terrassa

Unknown

Lidocaine-Prilocaine (EMLA) Cream as Analgesia in Hysterosalpingography Practice (HSG-2010)

Gynecological Pathology

Spain
Astellas Pharma Inc

Completed

Mass Balance Study of ASP1941

Healthy Subjects

Netherlands
Universidad Nacional de Rosario

Completed

Effectiveness of Dextrose Injection for Osgood-Schlatter Disease

Osgood-Schlatter Disease

Argentina
Astellas Pharma Inc

Completed

Drug-drug Interaction Study With ASP1941 and Glimepiride

Healthy Subjects

Netherlands
ConvaTec Inc.

Completed

AQUACEL® Ag Dressing and Urgotul® Silver Dressing on Healing of Chronic Venous Leg Ulcers

Leg Ulcer

Denmark, France, Germany, Poland, United Kingdom
Assistance Publique - Hôpitaux de Paris

Completed

Safety and Efficacy Study of Intravenous Lidocaine After Colorectal Surgery: LIDOREHAB

Colorectal Neoplasms

France
Chung-Ang University Hosptial, Chung-Ang University...

Unknown

The Effect of Intravenous Lidocaine on Pain After Tonsillectomy

Postoperative Pain

Korea, Republic of
University Health Network, Toronto

Completed

Venlafaxine Versus Lamotrigine in the Treatment of Bipolar I/II Depression

Bipolar Disorder

Canada
Astellas Pharma Inc

Completed

Multiple Dose Escalating Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ASP1941

Healthy

Netherlands
Astellas Pharma Inc

Completed

First in Men Study of Single Oral Doses of ASP1941 in Healthy Subjects

Healthy

United Kingdom
Novartis

Completed

Follow-up Study of Safety of Enteric-coated Mycophenolate Sodium in Patients Who Successfully Completed Study CERL080A302

Renal Transplant
Novartis

Completed

Clinical Study to Evaluate the Tolerability, Safety and Efficacy of Enteric-coated Mycophenolate Sodium After Equimolar Conversion From Mycophenolate Mofetil (MMF) in Patients With Renal Transplant

Prevention of Acute Rejection After Kidney Transplantation
Novartis

Completed

Clinical Study to Evaluate the Tolerability, Safety and Efficacy of Enteric-coated Mycophenolate Sodium, After Equimolar Conversion From Mycophenolate Mofetil (MMF), in Patients With Stable Renal Transplant Receiving Tacrolimus

Prevention of Acute Rejection After Kidney Transplantation
Novartis

Completed

Follow-up Study of Safety of Enteric-coated Mycophenolate Sodium in Patients Who Successfully Completed Study CERL080A301

Renal Transplant
Novartis

Completed

Efficacy and Safety of Enteric-coated Mycophenolate Sodium (EC-MPS) in de Novo Kidney Transplant Recipients

De Novo Kidney Transplant Recipients
Novartis

Completed

Safety and Efficacy of Enteric-coated Mycophenolate Sodium (EC-MPS) Plus Valsartan in Patients With Kidney Transplants (MYTHOS

De Novo Renal Transplantation
Eisai Inc.

Completed

A Study to Investigate Use Patterns and Safety in Simulated Actual Over-the-counter (OTC) Use of Rabeprazole Sodium for the Treatment of Heartburn Symptoms

Frequent Heartburn

United States
Novartis

Completed

Extension Study on the Efficacy and Safety of Enteric-coated Mycophenolate Sodium Administered in de Novo Kidney Transplant Patients

De Novo Kidney Transplantation
Novartis

Completed

Extension Study to Assess Tolerability and Safety of Enteric-coated Mycophenolate Sodium in Renal Transplant Recipients Who Received Mycophenolate Mofetil

Renal Transplantation
Novartis

Completed

Extension Study on the Safety and Efficacy of Enteric-coated Mycophenolate Sodium in Kidney Transplant Recipients

Renal Transplantation
Novartis

Completed

Extension Study of Enteric-coated Mycophenolate Sodium in Combination With Full Dose or Reduced Dose Cyclosporine Microemulsion in Patients With de Novo Kidney Transplants

Renal Transplantation
Novartis

Completed

Study of Enteric-Coated Mycophenolate Sodium (EC-MPS) Plus Reduced-dose Cyclosporine Microemulsion (CsA-ME) Compared to EC-MPS Plus Standard Dose CsA-ME in Eldery de Novo Renal Transplant Recipients Treated With Basiliximab and Short-term Steroids

Denovo Renal Transplantation
Novartis

Completed

Extension Study of the Safety and Efficacy of Enteric-coated Mycophenolate Sodium in Kidney Transplant Recipients

Renal Transplantation
Novartis

Completed

Study of Enteric-coated Mycophenolate Sodium Maintenance Therapy in Patients With Renal Transplant Receiving Cyclosporine Microemulsion and Steroids,

Maintenance Renal Transplantation
Azidus Brasil

Unknown

Pharmacodynamics Aspects Of Porcine Heparin Sodium, Produced by Eurofarma, Compared Heparin Sodium, Produced by APP Pharmaceuticasls, in Patients With Chronic Renal Failure

Pharmacodynamics
Azidus Brasil

Unknown

Efficacy and Safety Clinical Trial of the Combination of Acetylsalicylic Acid, Sodium Bicarbonate and Citric Acid, Produced by Geolab Pharmaceutical Industries Ltd., Compared to Acetylsalicylic Acid (Aspirin ® - Bayer) in Patients With Episodic Tension-type Headache.

Treatment of Episodic Tension Headache

Brazil
Azidus Brasil

Unknown

Efficacy and Safety of Sodium Heparin in Patients Submitted to Heart Surgery Using Bypass

Cardiac Surgery

Brazil
Mahidol University

Unknown

Hydroxypropylmethylcellulose 0.3% and Sodium Hyaluronate 0.18% for Ocular Surface Disease in Glaucoma

Glaucoma | Ocular Surface Disease

Thailand
Dr. Reddy's Laboratories Limited

Completed

Bioequivalence Study of Pantoprazole Sodium DR Tablets 40 mg of Dr. Reddy's Laboratories Limited Under Fasting Condition

Fasting

India
AstraZeneca

Completed

Anastrozole Biphosphonate Study in Postmenopausal Women With Hormone-Receptor-Positive Early Breast Cancer (SABRE)

Breast Cancer

United States, South Africa, Spain, France, Netherlands, United Kingdom, Greece, Canada
Bristol-Myers Squibb

Terminated

Safety Study of BMS-844421 for Treatment of Hypercholesterolemia

Atherosclerosis | Hypercholesterolemia

Germany
Dr. Reddy's Laboratories Limited

Completed

Bioequivalence Study of Pantoprazole Sodium DR Tablets 40 mg of Dr. Reddy's Laboratories Limited Under Fed Condition

FED

India
Aga Khan University

Completed

Intraperitoneal Analgesia After Laparoscopic Cholecystectomy

Laparoscopic Cholecystectomy

Pakistan
Cady, Roger, M.D.
GlaxoSmithKline

Completed

"Completeness of Response" Following Treatment With Treximet™ for Migraine

Migraine

United States
University of Roma La Sapienza

Completed

Topical Application of GTN 0.4% in the Treatment of Anismus Following Stapled Haemorrhoidopexy (TAGASH)

Pain After Stapled Haemorrhoidopexy

Italy
Amgen

Completed

A Randomized, Double-Blind Study to Compare the Efficacy of Treatment With Denosumab Versus Alendronate Sodium in Postmenopausal Women With Low Bone Mineral Density.

Osteoporosis | Osteopenia
AstraZeneca

Completed

An Open-label, Exploratory Trial to Assess Gastric Acid Control in Critically Ill Subjects Receiving Nexium

Gastric Ulcer

United States
McGill University Health Centre/Research Institute...

Completed

Intravenous Lidocaine for Laparoscopic Cholecystectomy

Postoperative Pain | Opioid Consumption

Canada
Sanofi

Completed

Fexofenadine HCl 180 mg, Montelukast Sodium 10 mg and Placebo in Suppression of Wheal and Flare Induced by Seasonal Allergen

Allergic Rhinitis

United States
Sanofi
Procter and Gamble

Completed

OPTAMISE: Clinical Effectiveness of Teriparatide After Alendronate or Risedronate Therapy in Osteoporotic Postmenopausal Women

Osteoporosis, Postmenopausal

United States, Netherlands, Australia, Belgium, Canada, France, United Kingdom
Sanofi

Completed

PREVAIL: PREvention of VTE After Acute Ischemic Stroke With LMWH Enoxaparin ( - VTE: Venous Thromboembolism - LMWH: Low Molecular Weight Heparin)

Acute Ischemic Stroke

Korea, Republic of, Italy, Brazil, Canada, Colombia, Israel, Mexico, Poland, Czech Republic, United States, Australia, Austria, India, South Africa, Turkey
Sanofi

Completed

EXCLAIM:Extended Prophylaxis for Venous ThromboEmbolism (VTE) in Acutely Ill Medical Patients With Prolonged Immobilization

Venous Thromboembolism

France, Russian Federation, Spain, Italy, Argentina, Belgium, Brazil, Canada, Colombia, Germany, Israel, Mexico, Poland, United States, Australia, Austria, India, South Africa, United Kingdom, Tunisia
Sanofi

Completed

HUPS: Hyalgan Use in Painful Shoulder

Osteoarthritis of Shoulder

United States
Sanofi

Completed

Safety Study of Sodium Divalproate in Bipolar Disorder in Adolescents (ADOKOT)

Bipolar Disorder

France
University Health Network, Toronto

Completed

Analysis of the Effect of Intravitreal Dexamethasone Injection on Diabetic Macular Edema After Cataract Surgery (IDDMECS) (IDDMECS)

Diabetes | Macular Edema | Pseudophakia

Canada
Sanofi

Completed

Safety and Efficacy of Enoxaparin in Percutaneous Coronary Intervention (PCI) Patients, an International Randomized Evaluation (STEEPLE)

Percutaneous Coronary Intervention
McMaster University
Canadian Institutes of Health Research (CIHR); Australian and New Zealand Intensive... and other collaborators

Completed

PROphylaxis for ThromboEmbolism in Critical Care Trial (PROTECT)

Critical Illness | Deep Venous Thrombosis

United States, Australia, Canada, Saudi Arabia, Brazil, United Kingdom

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