Search clinical trials for: Teicoplanin powder

Total 1527 results

Barts & The London NHS Trust

Completed

Vitamin D, Chronic Kidney Disease (CKD) and the Microcirculation

Vitamin D Deficiency | Chronic Kidney Disease

United Kingdom
Aerovance, Inc.

Completed

A Study of the Treatment-Sparing Effects of AEROVANT™ AER 001 Inhalation Powder in Asthma Patients, AEROTRIAL

Asthma

United States, United Kingdom, Hungary, Poland
Pfizer

Completed

A Study To Estimate The Time Course Of PF-00241939 Concentration In The Blood After Dosing With Oral Inhalation From Dry Powder Inhalers

Pharmacokinetics

Singapore
Chulalongkorn University

Unknown

Lime Powder Regimen in Healthy Volunteers (LimePKphase1)

Oxidative Stress | Kidney Stone

Thailand
Chinese University of Hong Kong

Unknown

Whole Soy and Daidzein on Reduction of Blood Pressure in Postmenopausal Chinese Women

Hypertension

China
Heidelberg University

Unknown

Therapy of Peri-implantitis: Scaling Versus Low Abrasive Powder

Peri-implantitis
Abbott Nutrition

Terminated

Growth and Tolerance of Healthy Term Infants to a New Infant Formula

Healthy Term Infants

United States
Eli Lilly and Company
Alkermes, Inc.

Completed

A Study for Patients With Type 1 Diabetes Mellitus

Diabetes Mellitus, Type 1

Japan, Taiwan
Louisville Metabolic and Atherosclerosis Research...
Daiichi Sankyo, Inc.; Provident Clinical Research

Completed

Comparison of Colesevelam Hydrogen Chloride (HCl) Powder For Oral Suspension Versus Generic Cholestyramine Through Use of the Bile Acid Sequestrant Acceptability (BASA) Scale

Healthy

United States
Charite University, Berlin, Germany
NSA, Collierville, TN, USA

Completed

Encapsulated Juice Powder Concentrate for Preventing Common Cold Symptoms

Common Cold

Germany
Hadassah Medical Organization

Completed

Bovine Colostrum for Patients With Non Alcoholic Fatty Liver Disease

Nonalcoholic Steatohepatitis | Fatty Liver Disease

Israel
Mead Johnson Nutrition

Completed

Feeding Study in Premature Infants

Premature Infants

United States
MicroDose Defense Products L.L.C.
University of Pittsburgh; U.S. Army Space and Missile Defense Command

Completed

A Study of Inhaled Atropine Sulfate in Healthy Adults

Organophosphorus Poisoning

United States
Solvay Pharmaceuticals

Completed

Safety and Efficacy of PROMETRIUM® Capsules in Induction of Secretory Conversion

Secondary Amenorrhea

United States
Pharmaxis

Completed

Long Term Administration of Inhaled Dry Powder Mannitol In Cystic Fibrosis - A Safety and Efficacy Study

Cystic Fibrosis

Ireland, United Kingdom, Australia
Meir Medical Center

Completed

Dehydroepiandrosterone Supplementation for Poor Responder Patients During in Vitro Fertilization Treatment

Ovarian Stimulation

Israel
Pfizer

Completed

An Open Label, Randomized, Crossover Study To Estimate The Pharmacokinetics And Evaluate The Safety Following A Single Dose Of Azithromycin 2g Extended-Release Powder For Oral Suspension With A 3-Day Dosing Regimen Of Azithromycin 500mg Tablet In Chinese Healthy Male Subjects

Healthy Volunteers

China
Research in Real-Life Ltd
Mundipharma Research Limited

Completed

Real-world Effectiveness of Combination Therapy in Asthma

Asthma

United Kingdom
Orion Corporation, Orion Pharma

Completed

Inspiratory Flow Parameters and Handling of Easyhaler and Turbuhaler Inhalers (PIFECO)

Pulmonary Disease, Chronic Obstructive | Asthma

United Kingdom, Finland
Anesiva, Inc.
Covance

Terminated

Satisfaction With Pediatric Intravenous Catheter Placement in the Emergency Department

Intravenous Placement Procedure
University of California, Davis
United States Agency for International Development (USAID)

Completed

Acceptability of Nutrient Supplements Among Women and Children in Bangladesh

Malnutrition

Bangladesh
Tibotec Pharmaceuticals, Ireland

Completed

TMC435350-TiDP16-C106: A Phase I Trial to Compare the Bioavailability and Plasma Pharmacokinetics After a Single Oral Dose of TMC435350 of 2 Different Solid Formulations Relative to a Powder Blend Capsule

Hepatitis C | HCV
Pfizer

Completed

Assessment Of The Inhalation Profiles Of Four Dry Powder Inhalers In Patients With Variable Degrees Of Lung Obstruction

Pulmonary Disease, Chronic Obstructive | Asthma

Germany
Pfizer

Completed

Study To Estimate The Time Course Of PF-04764793 In The Blood Following Dosing By Oral Inhalation From Dry Powder Inhalers

Healthy

Singapore
Pharmaxis

Completed

A Phase 2 Study to Determine the Safety and Efficacy of Inhaled Dry Powder Mannitol in Cystic Fibrosis

Cystic Fibrosis

Australia, New Zealand
Pfizer

Completed

Exubera Large Simple Trial To Evaluate Long-Term Pulmonary And Cardiovascular Safety (VOLUME)

Diabetes Mellitus

United States, Germany, Sweden, United Kingdom, Puerto Rico
innoVactiv Inc.

Completed

Safety and Efficacy of a Single Dose of a Polyphenol-enriched Brown Seaweed Powder in Human (ICAST)

Glycemic Index

Canada
National Center for Complementary and Integrative...

Completed

Identifying the Anti-Blood-Clotting Compounds in Garlic

Arteriosclerosis | Intracranial Arteriosclerosis

United States
Fred Hutchinson Cancer Center
National Center for Complementary and Integrative Health (NCCIH)

Completed

Effects of Garlic Supplements on Drug Metabolism

Healthy

United States
Pfizer

Completed

A Study Estimating The Time Course Of PF-04764793 In The Blood Following Dosing By Oral Inhalation From Dry Powder Inhalers

Healthy

Singapore
Silliker, Inc.
National Center for Complementary and Integrative Health (NCCIH)

Unknown

Allicin Bioavailability From Garlic Supplements and Garlic Foods

Healthy

United States
Mannkind Corporation

Completed

Comparison Between Technosphere/Insulin Inhalation Powder Versus Rapid Acting Insulin in Subjects With Type 2 Diabetes Mellitus

Diabetes Type 2

Russian Federation
Pharmaxis

Completed

A Pilot Study to Investigate Administration of Mannitol Via a Novel Dry Powder Inhaler Device

Healthy | Bronchiectasis

Australia
Hadassah Medical Organization

Unknown

VSL#3 Treatment in Children With Crohn's Disease

Crohn's Disease

Israel
Orion Corporation, Orion Pharma

Completed

Pharmacokinetic Pilot Study on Budesonide/Formoterol Device-metered Dry Powder Inhaler

Healthy

Finland
The Korean Society of Ginseng

Completed

Effect of Korean Red Ginseng (KRG) on Dry Mouth

Xerostomia

Korea, Republic of
Pfizer

Completed

A Study to Estimate the Time Course of PF-00241939 Concentration in the Blood Following Dosing by Oral Inhalation From Dry Powder Inhalers (B0871003)

Pharmacokinetics

Singapore
All India Institute of Medical Sciences, New Delhi

Unknown

A Study to Assess the Anti-Emetic Efficacy of Ginger in Children and Adolescents Receiving Chemotherapy

Nausea | Vomiting

India
Mannkind Corporation

Completed

Clamp Study Comparing Inhalation of Technosphere®/Insulin in Smokers and Non-Smokers With Type 2 Diabetes

Diabetes Type 2

United States
Pfizer

Completed

A Study To Estimate The Time Course Of PF-00241939 Concentration In The Blood Following Dosing By Oral Inhalation From Dry Powder Inhalers. (B0871002)

Healthy

Singapore
University of Illinois at Urbana-Champaign

Completed

Higher Protein Diet and Exercise for Optimal Weight Loss in Elderly Women

Quality of Life | Obesity | Metabolic Syndrome | Physical Function | Bone and Body Composition

United States
PETHEMA Foundation

Completed

Meropenem Versus Meropenem Plus Glycopeptide in Patients With Febrile Neutropenia After Allogenic Blood Stem Cell Transplantation (MERONEM)

Febrile Neutropenia | Allogenic Blood Stem Cell Transplantation

Spain
Sanofi

Completed

Comparison of Teicoplanin and Vancomycin in Initial Empirical Antibiotic Regimen for Febrile Neutropenic Patients

Febrile Neutropenia | Infection

Turkey
TorreyPines Therapeutics

Completed

A Safety Tolerance and Experimental Hyperalgesia Study of Oral NGX426 in Healthy Male Voluneteers

Healthy | Hyperalgesia

United States
Universidad Autónoma de Querétaro
Procter and Gamble

Completed

Evaluation of the Efficacy of Different Strategies to Treat Anemia in Mexican Children

Anemia
PowderMed

Completed

Safety Study of HBV DNA Vaccine to Treat Patients With Chronic Hepatitis B Infection

Chronic Hepatitis B

Thailand, Hong Kong, Singapore, Taiwan
PowderMed

Completed

A Safety Study to Assess a DNA Vaccine Administered by Particle Mediated Delivery to the Skin in Healthy Subjects

HSV-2

United States
Aerovance, Inc.

Completed

A Phase 1 Safety and Pharmacokinetics Study of AER 001 Administered as a Dry Powder in Asthmatic Subjects

Asthma

United Kingdom
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Cefprozil 250 mg/ 5mL Powder For Oral Suspension Under Fasting Conditions

Healthy

Canada
Ranbaxy Laboratories Limited

Completed

Bioequivalence Study of Cefprozil 250 mg/ 5mL Powder For Oral Suspension Under Fed Conditions

Healthy

Canada

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