Search clinical trials for: TOS-358

Total 2705 results

Totus Medicines

Recruiting

A Study to Evaluate the Safety and Tolerability of TOS-358 in Adults With Select Solid Tumors

Cervical Cancer | Gastric Cancer | Colorectal Cancer | Ovarian Cancer | Squamous Cell Carcinoma of Head and Neck | Endometrial Cancer | Non-small Cell Lung Cancer | Urothelial Carcinoma | HER2-negative Breast Cancer

United States
Christian Ruff

Not yet recruiting

Brain Network Mechanisms Causally Underlying Human Decisions Revealed by Brain Stimulation and Functional MRI

Behavior and Behavior Mechanisms
Universidad Nacional Andres Bello

Completed

Behavioral Therapy and Self-care vs Thermoformed Occlusal Splints in the Treatment of Masticatory Muscles Pain

Myalgia of Mastication Muscle

Chile
Boston Pharmaceuticals

Completed

Study to Evaluate the Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Effects of Repeat Topical Application of BOS-356 in Subjects With Moderate to Severe Acne Vulgaris

Moderate to Severe Acne Vulgaris

United States, Canada
Merve Erkmen Almaz
Kırıkkale University

Completed

Salivary TAS, TOS, LL-37 and Dental Status in Passive Smoking Children

Dental Caries | Children | Oxidative Stress | Passive Smoking
Gopalkumar Rakesh
National Cancer Institute (NCI)

Recruiting

Accelerated Transcranial Magnetic Stimulation (TMS) for Smoking Cessation in People Living With HIV/AIDS (PLWHA)

Tobacco Smoking | Hiv

United States
Merve Erkmen Almaz
Kırıkkale University

Completed

Effect of Passive Smoking on Oxidative Stress and Dental Caries in Children

Dental Caries | Oxidative Stress | Passive Smoking
Kaleido Biosciences

Completed

Study to Evaluate the Tolerability of Prebiotics on the Microbiota

Healthy

Ireland
Milton S. Hershey Medical Center
National Institute on Drug Abuse (NIDA); National Institutes of Health (NIH); Food and Drug Administration (FDA)

Completed

Switching to Low Oxidant Content Cigarettes in Adult Smokers

Oxidative Stress | Nicotine

United States
Wageningen University

Unknown

Fiber Fermentation, and Short Chain Fatty Acid Kinetics and Utilization Inside the Gut and Systemic Circulation

Dietary Fiber

Netherlands
Hôpital le Vinatier

Completed

Intermittent Theta Burst Stimulation (iTBS) for the Treatment of Negative Symptoms in Schizophrenia

Schizophrenia

France
The Royal Ottawa Mental Health Centre

Not yet recruiting

Comparing the Efficacy of fMRI-Guided vs. Standard iTBS in Treating Depression

Depression | Depressive Disorder, Major | Depressive Episode

Canada
Masaryk University
Swiss Federal Institute of Technology

Recruiting

Novel, Individualized Brain Stimulation, Network-based Approaches to Improve Cognition (NiBS-iCog)

Healthy Aging | Mild Cognitive Impairment

Czechia
University of Warmia and Mazury in Olsztyn
Regional Specialized Hospital in Olsztyn

Completed

: A Comparison of Neuromuscular Transmission in the Muscles During General Anesthesia

Neuromuscular Blockade

Poland
Bird, Christopher
London School of Hygiene and Tropical Medicine; Fondazione Ivo de Carneri,...

Completed

Study to Test Whether Shoes Protect Children Against Hookworm Infection on Pemba Island, Zanzibar (SKIP)

Hookworm

Tanzania
Nektar Therapeutics
Eli Lilly and Company

Completed

A Study of LY3471851 in Participants With Psoriasis

Psoriasis

United States
Nektar Therapeutics
Eli Lilly and Company

Completed

A Study of LY3471851 in Healthy Participants

Healthy

United States
Talima Therapeutics, Inc.

Terminated

A Study to Evaluate TMI-358 in the Treatment of Distal Subungual Onychomycosis

Distal Subungual Onychomycosis

United States
XOMA (US) LLC

Completed

An Open-Label Study of XOMA 358 in Patients With Hypoglycemia After Gastric Bypass Surgery (XOMA 358)

Hypoglycemia

United States
University of California, Los Angeles
National Institute of Mental Health (NIMH)

Completed

Four-week Open-trial Extension TNS for ADHD

Attention Deficit Hyperactivity Disorder (ADHD)

United States
Children's Hospital Medical Center, Cincinnati

Completed

Repetitive Transcranial Magnetic Stimulation to Reduce Tics

Tourette Syndrome

United States
Nektar Therapeutics
Eli Lilly and Company

Completed

A Study of LY3471851 in Participants With Eczema

Dermatitis, Atopic

United States
AbbVie (prior sponsor, Abbott)
Massachusetts General Hospital

Completed

The PRIMO Study: Paricalcitol Capsules Benefits Renal Failure Induced Cardiac Morbidity in Subjects With Chronic Kidney Disease Stage 3/4 (PRIMO)

Chronic Kidney Disease | Left Ventricular Hypertrophy

United States, Australia, Czech Republic, Germany, Italy, Poland, Puerto Rico, Romania, Russian Federation, Spain, Taiwan, United Kingdom
Danish Headache Center

Completed

Assessment of ICP in Idiopathic Intracranial Hypertension Using Transocular Ultrasound and Transcranial Doppler

Idiopathic Intracranial Hypertension

Denmark
Medical College of Wisconsin

Recruiting

Gastroschisis Outcomes of Delivery (GOOD) Study

Gastroschisis

United States
Queen Margaret University

Not yet recruiting

Inter-rater Reliability of Diagnosing Thoracic Outlet Syndrome by Physiotherapists

Thoracic Outlet Syndrome
Abbott

Completed

Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyroid Hormone in Chronic Kidney Disease

Chronic Kidney Disease

China
Nektar Therapeutics
Eli Lilly and Company

Completed

A Study of NKTR-358 (LY3471851) in Participants With Systemic Lupus Erythematosus (SLE)

Systemic Lupus Erythematosus

United States
Johnson & Johnson Consumer and Personal Products...
Fudan University; Beijing Children's Hospital; Shanghai China-Norm Management... and other collaborators

Completed

A Clinical Assessment of the Efficacy and Effects of Different Skincare Regimens on Infants

Baby Skin Development

China
Nektar Therapeutics
Eli Lilly and Company

Terminated

A Study of LY3471851 in Adult Participants With Moderately to Severely Active Ulcerative Colitis (UC) (INSTRUCT-UC)

Colitis, Ulcerative

Australia, India, United States, Korea, Republic of, Hungary, United Kingdom, Japan, Argentina, Belgium, Brazil, Canada, China, Czechia, France, Georgia, Israel, Latvia, Poland, Romania, Russian Federation, Slovakia, Ukraine
Nektar Therapeutics
Eli Lilly and Company

Completed

A Study of NKTR-358 (LY3471851) in Healthy Participants

Healthy

United States
European Organisation for Research and Treatment...

Recruiting

Study Assessing The "Best of" Radiotherapy vs the "Best of" Surgery in Patients With Oropharyngeal Carcinoma (Best Of)

Oropharyngeal Cancer | Hypopharyngeal Squamous Cell Carcinoma | Supraglottic Squamous Cell Carcinoma

Spain, Belgium, Switzerland, Italy, United Kingdom, Germany, France, Poland
University of Tehran

Unknown

Repetitive Transcranial Magnetic Stimulation and Intermittent Theta Burst (iTBS) in Schizophrenia

Schizophrenia

Iran, Islamic Republic of
Abbott
Abbott Japan Co.,Ltd

Completed

Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Patients With Hemodialysis (HD)

Hemodialysis | Secondary Hyperparathyroidism

Japan
Nektar Therapeutics

Recruiting

A Phase 2b Study to Evaluate Rezpegaldesleukin (Rezpeg) in the Treatment of Severe to Very Severe Alopecia Areata in Adult Patients (Rezolve AA)

Alopecia Areata

United States
Nektar Therapeutics
Eli Lilly and Company

Completed

A Study of LY3471851 in Adults With Systemic Lupus Erythematosus (SLE) (ISLAND-SLE)

Systemic Lupus Erythematosus

United States, Spain, Japan, India, Israel, Korea, Republic of, Taiwan, Australia, Puerto Rico, Argentina, Romania, Canada, Germany, Russian Federation, Mexico, Ukraine, Poland, Czechia, Hungary
Agios Pharmaceuticals, Inc.

Completed

A Study to Evaluate the Absorption, Distribution, Metabolism, Excretion and Absolute Bioavailability of AG-348 in Healthy Male Participants Following Administration of a Single Oral Dose of [14C]AG-348 and Concomitant Single Intravenous Microdose of [13C6]AG-348

Healthy Volunteers

United States
MedImmune LLC
AstraZeneca; MedImmune Ltd

Completed

A Study to Assess the Safety and Immunogenicity of the Drug CAT-354 in Healthy Japanese Subjects

Healthy

United States
Hartford Hospital

Recruiting

Can Transcranial Magnetic Stimulation Decrease Food Reinforcement

Obesity

United States
Carilion Clinic

Unknown

Transcranial Magnetic Stimulation (TMS) for Trigeminal Neuralgia (TGN)

Facial Pain

United States
Nektar Therapeutics

Recruiting

A Phase 2b Study to Evaluate Rezpegaldesleukin (Rezpeg) in the Treatment of Adult Patients With Moderate-to-Severe Atopic Dermatitis (REZOLVE-AD)

Moderate to Severe Atopic Dermatitis

United States, Australia, Canada
University of Southern California

Not yet recruiting

Transcranial Magnetic Stimulation for Binge Eating Disorder (TMS for BED)

Binge-Eating Disorder
Travere Therapeutics, Inc.

Active, not recruiting

Pegtibatinase as an Enzyme Therapy for Patients With Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (COMPOSE)

Homocystinuria

United States
Global Alliance for TB Drug Development

Terminated

A Multiple Ascending Dose Study With a Dose Formulation Comparison Cohort to Evaluate the Safety, Tolerability, and Pharmacokinetics of TBA-354 in Healthy Adult Subjects

Tuberculosis
Emory University

Completed

Cortical Contributions to Motor Sequence Learning

Brain Injuries

United States
University of North Carolina, Chapel Hill
National Institute of Mental Health (NIMH)

Completed

Modulation of Cognitive Control Signals in Prefrontal Cortex by Rhythmic Transcranial Magnetic Stimulation

Executive Function

United States
Xinqiao Hospital of Chongqing

Completed

3DV+TPS Applied to Radiotherapy for Nasopharyngeal Carcinoma

Nasopharynx Cancer | Radiotherapy

China
Bayside Health
National Health and Medical Research Council, Australia

Completed

A Double-blind Sham Controlled Trial of rTMS in Treatment Resistant Major Depression

Major Depressive Disorder

Australia
Bayside Health

Completed

rTMS in the Treatment of Bipolar Depression

Bipolar Affective Disorder

Australia
Travere Therapeutics, Inc.

Recruiting

A Study to Investigate Efficacy and Safety of Pegtibatinase Compared With Placebo in Participants ≥12 to ≤65 Years of Age With Classical Homocystinuria (HCU) Due to Cystathionine Beta Synthase Deficiency Receiving Standard of Care Treatment (HARMONY)

Homocystinuria

United States

Search clinical trials for: TOS-358

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