Search clinical trials for: AZD7442 IV

Total 3259 results

Eli Lilly and Company

Completed

A Relative Bioavailability Study of LY3209590 in Healthy Participants

Healthy

Singapore
Duke University

Completed

Ipsilateral Peripheral Intravenous Access Procedures (The iPIVAP Study) (iPIVAP)

Melanoma | Breast Cancer | Lymphedema of Upper Arm | Thoracic Cancer

United States
Tufts Medical Center
Baystate Medical Center

Completed

Single-operator Ultrasound-guided IV Placement by Emergency Nurses

Intravenous Infusions

United States
Aarhus University Hospital

Terminated

The Predictive Performance of Renal Ultrasound on Changes in Renal Clearance

Acute Kidney Injury | Fluid Overload | Hypoperfusion

Denmark
St George's Healthcare NHS Trust

Unknown

Response to Varying the Rate of Administration of a Fluid Challenge

Peri-operative Fluid Management
Pacira CryoTech, Inc., a wholly owned subsidiary...

Completed

A Prospective Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the Cryo-Touch IV Device

Glabellar Frown Lines | Frown Lines

United States
Wockhardt

Completed

Phase I, Open Label,Crossover Food-Effect and Absolute Bioavailability Study of WCK2349 and WCK771 in Healthy Adult Human Volunteers

Effect of Food

United States
Cancer Research UK

Terminated

A Phase I Study of AZD0424 Alone and in Combination in Advanced Solid Tumours (AZD0424)

Advanced Solid Tumours

United Kingdom
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
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
Rambam Health Care Campus

Completed

IV Iron in Acute Decompensated Heart Failure

Heart Failure

Israel
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
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
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
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
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
Mallinckrodt

Completed

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

Fever | Acute Pain

United States
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
Protgen Ltd

Unknown

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

Advanced Solid Tumors

China
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
The Netherlands Cancer Institute
Leiden University Medical Center; University Medical Center Nijmegen

Recruiting

Sarcomas and DDR-Inhibition; a Combined Modality Study (SADDRIN-1)

Soft Tissue Sarcoma Adult

Netherlands
Naurex, Inc, an affiliate of Allergan plc

Terminated

Open Label Extension for GLYX13-C-202, NCT01684163

Major Depressive Disorder

United States
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

Search clinical trials for: AZD7442 IV

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