Search clinical trials for: RoActemra iv

Total 3480 results

Merck Sharp & Dohme LLC

Not yet recruiting

A Study to Evaluate the Efficacy and Safety of Tulisokibart (MK-7240) in Participants With Moderate to Severe Crohn's Disease (MK-7240-008)

Crohn's Disease
Merck Sharp & Dohme LLC
PPD, Part of Thermo Fisher Scientific

Recruiting

A Study to Evaluate Efficacy and Safety of Tulisokibart (MK-7240) in Participants With Moderately to Severely Active Ulcerative Colitis (MK-7240-001)

Ulcerative Colitis

United States, Israel, Japan, Korea, Republic of, Switzerland, Chile, Dominican Republic, Canada, Netherlands
BioMarin Pharmaceutical

Terminated

Open Label, Extension Study of PRO044 in Duchenne Muscular Dystrophy (DMD)

Duchenne Muscular Dystrophy

Belgium, Netherlands, Italy, Sweden
Bioblast Pharma Ltd.
Parexel

Completed

A Study to Establish Safety and Maximum Tolerated Dose of IV Trehalose in Healthy Subjects

Healthy Volunteer Subjects

United States
C. R. Bard

Completed

Comparison of AccuCath IV Catheter and Conventional IV Catheter in Interventional Radiology

Vascular Access Complications

United States
C. R. Bard

Completed

Prospective Feasibility Trial of AccuCath 2.25" Blood Control (BC) Placed in Difficult Access Patients in the Emergency Department

Vascular Access Complication

United States
Centre Hospitalier Intercommunal de Toulon La Seyne...
Sainte-Anne Military Teaching Hospital

Completed

Drug Wastage : Observational Study in Intensive Care Units in France (GAME-OVER)

Drug Use

France, Monaco, Mayotte
H. Lundbeck A/S

Completed

Study With Lu AF35700 in Healthy Men and Women in Fasting and Fed State

Healthy

United Kingdom
Hoffmann-La Roche

Completed

A Study of Subcutaneously Administered Tocilizumab in Patients With Rheumatoid Arthritis

Rheumatoid Arthritis

Canada, New Zealand, Spain
Hoffmann-La Roche

Completed

Study to Evaluate the Safety, Tolerability and Efficacy of Tocilizumab in Participants With Rheumatoid Arthritis (RA) Who Have an Inadequate Response to Non-Biologic Disease Modifying Anti-rheumatic Drugs (DMARDs) and/or Anti-tumor Necrosis Factor (Anti-TNF) Therapy

Rheumatoid Arthritis

India
Rambam Health Care Campus

Completed

IV Iron in Acute Decompensated Heart Failure

Heart Failure

Israel
Arizona State University

Not yet recruiting

Rehydration Efficiency During Ad-libitum Fluid Intake (LIV-D2O)

Dehydration

United States
Amgen

Terminated

Study to Evaluate the Safety and Tolerability of AMG 986 in Healthy Volunteers and Heart Failure Patients

Heart Failure | Healthy Volunteer

France, United States, Netherlands, New Zealand, Germany, Australia, Poland, Canada, Singapore
Pfizer

Completed

Special Investigation Of Azithromycin IV For Legionnaires' Disease (Regulatory Post Marketing Commitment Plan) (RESCUE-L)

Legionnaires' Disease | Legionella Pneumophila Infections
National University Hospital, Singapore

Unknown

The Role of Intravenous Albumin Replacement During Abdominal Paracentesis in Patients With Malignancy Related Ascites

Ascites | Hypotension

Singapore
Hoffmann-La Roche

Completed

An Extension Study of Tocilizumab (Myeloma Receptor Antibody [MRA]) in Patients Completing Treatment in Tocilizumab Core Studies

Rheumatoid Arthritis

France, Germany, Italy, Spain, Sweden, China, United States, Australia, Canada, Mexico, South Africa, United Kingdom, Czech Republic, Finland, Russian Federation, Switzerland, Thailand, Belgium, Denmark, Slovenia, Serbia, Israel, Hong... and more
Hoffmann-La Roche

Completed

EMBRACE-SC: Observational Study of Subcutaneous (SC) Tocilizumab Alone or in Combination With Conventional Disease-Modifying Antirheumatic Drugs (cDMARDs) in Rheumatoid Arthritis

Rheumatoid Arthritis

Greece
William Beaumont Hospitals

Completed

Ultrasound Guided Catheter Length Survivability

Catheter Complications

United States
Pfizer

Completed

Drug Use Investigation Of Azithromycin IV For Pneumonia Or Pelvic Inflammatory Disease (Regulatory Post Marketing Commitment Plan) (RESCUE)

Pneumonia | Pelvic Inflammatory Disease
Anglo-European College of Chiropractic

Unknown

Comparison of a Multiple Thrust Instrument to a Single Thrust Instrument in Treating the Low Back (AECC)

Low Back Pain

United Kingdom
International AIDS Vaccine Initiative
Beth Israel Deaconess Medical Center, Boston MA; Ragon Institute of MGH, MIT... and other collaborators

Completed

Safety, PK and Antiviral Activity of PGT121 Monoclonal Antibody in HIV-uninfected and HIV-infected Adults

HIV Infection

United States
Cara Therapeutics, Inc.

Completed

A Study Evaluating the Overall Pain Relief and Safety of Intravenous (IV) CR845 in Patients Undergoing Abdominal Surgery

Post Abdominal Surgery Pain

United States
Mallinckrodt

Completed

Safety and Efficacy of Intravenous Acetaminophen (IV APAP) in Adult Inpatients

Fever | Acute Pain

United States
Fu-Dong Shi

Completed

A Longitudinal Study of ACTEMRA® (Tocilizumab) as Monotherapy in Highly Active NMOSD

Neuromyelitis Optica | Neuromyelitis Optica Spectrum Disorders | Devic's Disease

China
Weill Medical College of Cornell University

Terminated

Phase II Study of Tocilizumab for Patients With Glucocorticoid-refractory Acute GVHD After Allogeneic Hematopoetic Stem Cell Transplant (HSCT)

Glucocorticosteroid Refractory Acute GVHD

United States
Sanofi

Active, not recruiting

Proof-of-concept Study for SAR441344 (Frexalimab) in Relapsing Multiple Sclerosis

Multiple Sclerosis

Bulgaria, Canada, Turkey, Spain, United States, Czechia, France, Germany, Russian Federation, Ukraine
Protgen Ltd

Unknown

Dose Escalation and PK Study of M2ES in Subjects With Advanced Solid Tumors

Advanced Solid Tumors

China
Centocor, Inc.

Completed

A Study of Safety and Effectiveness of Ustekinumab in Patients With Moderate to Severe Active Crohn's Disease Who Have Been Previously Treated With Anti-TNF Therapy

Crohn's Disease

United States, France, United Kingdom, Germany, Spain, Belgium, Israel, Australia, Canada, Netherlands, New Zealand, Austria
University Hospital, Grenoble

Not yet recruiting

Study of Functional and Aesthetic Outcomes After Wassel IV Thumb Duplication Surgery in Pediatric Population, With a Follow-up of at Least One Year

Wassel IV Thumb Duplication
University of Alabama at Birmingham
Michael J. Fox Foundation for Parkinson's Research

Not yet recruiting

Longitudinal TSPO PET Imaging With [18F]DPA-714 in PPMI (PPMI DPA-714 PET Imaging)

Parkinson Disease

United States
Masonic Cancer Center, University of Minnesota

Recruiting

MT2022-01: MSCs for ALD

Cerebral Adrenoleukodystrophy

United States
argenx

Completed

Evaluating the Pharmacodynamic Noninferiority of Efgartigimod PH20 SC Administered Subcutaneously as Compared to Efgartigimod Administered Intravenously in Patients With Generalized Myasthenia Gravis (ADAPTsc)

Generalized Myasthenia Gravis

Spain, United States, Belgium, Georgia, Germany, Hungary, Italy, Japan, Netherlands, Poland, Russian Federation
Ralph Beltran

Completed

Prospective Observational Study of Difficult Intravenous Access in the Operating Room

Difficult Intravenous Access

United States
Coopervision, Inc.

Completed

Clinical Performance of Habitual Wearers of Bioclear 1-day Lenses When Refitted With Biomedics 1-day Extra for 1 Week

Myopia | Hyperopia

Spain
Centre Hospitalier Universitaire, Amiens

Completed

Place of Echocardiography in IV Fluid Therapy in Patients With Septic Shock and Left Ventricular Systolic Dysfunction (DYSPRED)

Shock, Septic | Ventricular Dysfunction, Left

France
Singapore General Hospital
Singapore Civil Defence Force

Completed

Intraosseous vs Intravenous Access for Cardiac Arrest Treatment

Cardiac Arrest

Singapore
MedImmune LLC

Completed

To Evaluate Safety, Pharmacokinetics and Pharmacodynamics of MEDI6012 in Subjects With Stable Coronary Artery Disease

Coronary Artery Disease

United States
Healeon Medical Inc
Terry, Glenn C., M.D.

Enrolling by invitation

Use of Autologous, Adult Adipose-Derived Stem/Stromal Cells In Chronic Lung Disorders (ADcSVF-COPD)

Lung Disease

United States, Honduras
Aeglea Biotherapeutics

Terminated

A Multiple Ascending Dose Study of ACN00177 (Pegtarviliase) in Subjects With CBS Deficiency

Homocystinuria Due to Cystathionine Beta-Synthase Deficiency

United States, United Kingdom, Australia
argenx

Completed

A Phase 1 Study to Compare the Safety and Effect of Efgartigimod as an Intravenous Infusion With the Effect of Efgartigimod as a Subcutaneous Injection in Healthy Volunteers

Healthy Volunteers

Netherlands
Eli Lilly and Company

Completed

A Safety Study of LY3462817 in Healthy Participants

Healthy

Singapore
Brigham and Women's Hospital

Completed

Comparison of Ultrasound Guided Peripheral IV Placement With and Without Use of a Guidewire

Difficult Peripheral IV Access

United States
ClearLine MD

Completed

Factors Increasing Air Burden in Intravenous Tubing

Air Leakage | Air Embolism | Air Burden
Weill Medical College of Cornell University

Withdrawn

Laser Therapy in the Treatment of Post Thoracotomy Pain; A Pilot Study

Laser Therapy | Post Thoracotomy Pain

United States
University of Aarhus

Unknown

Ultrasound-guided Peripheral Vascular Access in Children

Ultrasonography | Pediatrics | Vascular Access Devices

Denmark
Jean Michel Hascoet
Maternite Regionale Universitaire

Completed

Prematurity Related Risks of Cognitive Impairment at School Age (NEORIS)

Complications of Prematurity

France
Bayside Health
National Health and Medical Research Council, Australia; Monash University; Cystic...

Unknown

Treatment of Metabolic Alkalosis in Acute Exacerbations of Cystic Fibrosis

Cystic Fibrosis

Australia
Naurex, Inc, an affiliate of Allergan plc

Terminated

Open Label Extension for GLYX13-C-202, NCT01684163

Major Depressive Disorder

United States
Hoffmann-La Roche

Completed

A Study to Evaluate the Use of Glucocorticoids in Combination With Tocilizumab in Daily Clinical Practice (COGNOS)

Rheumatoid Arthritis

Belgium
Jordi Gol i Gurina Foundation

Completed

Long-Term Survival After Ischaemic Stroke: Ebrictus Study (EBRICTUS)

Ischemic Stroke | Long Term Adverse Effects | Gender Bias | Thrombolytic (t-PA) Treatment

Spain

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