Search clinical trials for: Cameriere European Formula

Total 6915 results

Wuhan University
Peking University; Pfizer

Unknown

Efficacy and Safety of Ziprasidone to Treat Depressive Symptoms in Patients With Schizophrenia

The Primary Evaluation is the Change From Baseline at End of Study for CDSS Total Scores. | The Secondary Efficacy Evaluations Include: MADRS, PANSS Total Scores and Subscales and Responder Rate; CGI-S and CGI-I Scales. | Safety Evaluations Include: Laboratory Test Abnormalities; BARS... and other conditions
AstraZeneca

Completed

AZD 2066 Single Dose Formulation and Food Effect Study in Healthy Volunteers

Healthy
AstraZeneca

Completed

Formulation and Food Effect Study of AZD1386 in Healthy Volunteers

Pharmacokinetics
Sanofi

Terminated

European Trial About Effect of RimoNabant on Abdominal Obese Patients With dysLipidemia (ETERNAL)

Obesity | Dyslipidemias

Germany, Netherlands, Turkey, Slovakia, United Kingdom, Finland, Hungary, Ireland, Italy, Norway, Greece, Sweden, Czech Republic, Portugal, Switzerland
Renovo

Completed

A Trial to Compare the Efficacy of Two Formulations of Avotermin Against Placebo (RN1006)

Scar Improvement

United Kingdom
AstraZeneca
Scentryphar Clinical Research; Cori Analyticals; Clínica São Lucas, Hospital... and other collaborators

Completed

Evaluation of the Pharmacokinetic Interaction Between Candesartan and Felodipine After Ingestion of a Specific Meal

Healthy

Brazil
AstraZeneca

Completed

Evaluate Different Extended-release (ER) Tablets/Capsules of AZD1305 (2007-005765-38)

Healthy

United Kingdom
AstraZeneca

Completed

Study to Compare Different Formulations of AZD3355

Gastroesophageal Reflux Disease

Sweden
National Institute of Pediatrics, Mexico
Nekutli S.A. de C.V.

Completed

A Prebiotic Agave Derivated Metlin & Metlos in Infant Formula

Healthy Term Babies

Mexico
AstraZeneca

Completed

Single Ascending Dose Study (SAD) iv Formulation (2006-006253-27)

Healthy

Sweden
Italian Society of Nephrology
European Commission; Memorial University of Newfoundland

Terminated

Bicarbonate v Saline to Prevent Contrast Nephropathy

Kidney Failure, Acute | Contrast Media

Italy
China Medical University Hospital

Unknown

Establish the Caring Model of Children With Chronic Kidney Disease and End-stage Renal Disease: To Set up Childhood Glomerular Filtration Rate (GFR) Formula in Taiwan

Chronic Kidney Disease | End-Stage Renal Disease
Abbott Nutrition

Completed

Tolerance of Healthy Term Infants Fed Infant Formulas #3

Gastrointestinal Tolerance

United States
Abbott Nutrition

Terminated

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

Healthy Term Infants

United States
Abbott Nutrition

Completed

Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based Formulas With Different Fat Blends

Infant

Brazil
AstraZeneca

Completed

DIALOOG: Crestor in Patients With Diabetes Mellitus Type 2: Lowering of LDL-C Levels to New European Guidelines

Diabetes Mellitus Type 2 | LDL Cholesterol | Observational | Crestor, Rosuvastatin

Netherlands
University of Zurich
Ixodes GmbH; Appletree AG

Completed

Safety, Skin and Plasma Concentration of Azithromycin Dermal Formulation (IXO-01)

Lyme Disease

Switzerland
Tehran University of Medical Sciences

Unknown

Amantadine Versus Ritalin in the Treatment of Attention Deficit Hyperactivity Disorder (ADHD)

Attention Deficit Hyperactivity Disorder

Iran, Islamic Republic of
MedImmune LLC

Completed

A Phase II Randomized, Double-Blind, Two-Period Cross-Over Study to Evaluate the Pharmacokinetics, Safety and Tolerability of a Liquid Formulation of Palizvizumab (MEDI-493, Synagis)

-Unhealthy Children With a History of Prematurity

United States
Abbott
Genentech, Inc.

Completed

Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female Subjects

Healthy Female Subjects

United States
Essentialis, Inc.
Cetero Research, San Antonio

Completed

Open-label Pharmacokinetic Study of Diazoxide Choline Coated vs. Uncoated Formulations

Hypertriglyceridemia

United States
McMaster University
Ajinomoto USA, INC.

Completed

Impact of Varying Doses of Amino Acids on Exercise, Muscular and Mental Performance

Psychological Phenomena: Central Fatigue

Canada
Hunan University of Traditional Chinese Medicine

Unknown

Safety Study of a Chinese Herbal Formula Simotang Oral Liquid for the Treatment of Functional Dyspepsia (SMT)

Functional Dyspepsia(FD) Was Studied | Effect of Simotang on FD Was Studied

China
Ludwig-Maximilians - University of Munich
Sanofi; Merck Sharp & Dohme LLC; Pfizer; Hoffmann-La Roche

Completed

Cap/Iri Plus Cetuximab Compared to Cap/ox Plus Cetuximab in Patients With Metastatic Colorectal Cancer.

Metastatic Colorectal Cancer
Azidus Brasil

Unknown

Comparison of Two Heparin Formulations in Patients With Chronic Renal Failure. (HEPHIP0509)

Thrombus

Brazil
Abbott

Completed

Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compared to ABT-072 Capsule Formulation

Hepatitis C

United States
University of Edinburgh
NHS Lothian; European Society of Organ Transplantation

Completed

Liver Transplantation and Reticuloendothelial Clearance Capacity

Hepatic Insufficiency | Liver Insufficiency

United Kingdom
Abbott

Completed

Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulation and Safety, Tolerability and PK Study of Single Doses of ABT-333 in Healthy Volunteers

HCV Infection

United States
Puleva Biotech

Completed

Effect of a Follow on Formula With Lactobacillus Fermentum on the Incidence of Infections

Incidence of Infectious Diseases
Abbott
Genentech, Inc.

Completed

Assess the Oral Bioavailability of New ABT-263 Formulations

Chronic Lymphocytic Leukemia | Lymphomas | Leukemias

United States
Yazd Medical University
Yazd Research & Clinical Center for Infertility

Completed

Mild Stimulation Protocol Versus Microdose Gonadotropin-releasing Hormone Agonist Flare up Protocol in Poor Responders

Pregnancy

Iran, Islamic Republic of
PharmAthene, Inc.
National Institute of Allergy and Infectious Diseases (NIAID); National Institutes...

Completed

Study of Valortim® (MDX-1303) and Its Selected Formulation Components Percutaneous Use

Allergic Reactions

United States
Soroka University Medical Center
European Union

Completed

Self Mobility Improvement in the Elderly by Counteracting Falls (SMILING)

Falls

Israel
Mead Johnson Nutrition

Completed

Allergy and Ashthma in Children Who Were Fed Supplemented Infant Formula

Allergy and Asthma

United States
Pfizer

Completed

Pharmacokinetics And Safety Study Of Two CP-690,550 Controlled Release Formulation Following Single Dose In Healthy Volunteers

Healthy

Singapore
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Comparing Two Different Tablet Formulations Of Bosutinib Under Fed Conditions

Healthy

United States
South Eastern European Research Oncology Group
Roche Pharma AG

Unknown

Bevacizumab and Capecitabine in Treatment of Elderly Patients With Metastatic Breast Cancer

Breast Cancer | Metastasis

Croatia
Pfizer

Completed

A Phase 1 Study To Estimate The Relative Bioavailability Of Co-Administered Formulations Of Azithromycin Microsphere And Chloroquine Test Formulation Compared With Co-Administered Immediate Release Individual Azithromycin And Chloroquine Tablets In Healthy Adult Subjects (AZCQ)

Malaria Prophylaxis

United States
Abbott Nutrition

Completed

Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes

Diabetes Mellitus, Type 2

Russian Federation
Fresenius Kabi

Completed

The Effect of a New Specific Enteral Formula Compared to a Standard Formula on the Tolerability of a Combined Radio- and Chemotherapy in Cancer Patients

Enteral Nutrition

Germany
Seoul National University Hospital
Merck Sharp & Dohme LLC

Unknown

Study to Compare the Effect of Vytorin (Simvastatin/Ezetimibe) 10/20mg Versus Atorvastatin 20mg on ApoB/ApoA1 Ratio in Subjects With Diabetes

Type 2 Diabetes Mellitus Without Insulin Treatment

Korea, Republic of
Mead Johnson Nutrition

Completed

Double Blind Controlled Trial of an Extensively Hydrolyzed Formula With a Probiotic vs. an Extensively Hydrolyzed Formula Without a Probiotic

Allergy

Italy, Netherlands
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
Fernandes Tavora Hospital
Hospital Bandeirantes; Hospital Santa Luzia; Hospital Samaritano; Hospital da Polícia... and other collaborators

Completed

Evaluating the Influence of Ready-to-use (RTU) Parenteral Nutrition in the Clinical Outcome of Patients Study (EPICOS)

Parenteral Nutrition

Guatemala, Argentina, Brazil
Mead Johnson Nutrition

Completed

Evaluation of Mineral Absorption in Infants Fed Infant Formula

Mineral Absorption in the Urine

United States
Boston Scientific Corporation

Completed

Randomized Trial Evaluating Slow-Release Formulation TAXUS Paclitaxel-Eluting Coronary Stents to Treat De Novo Coronary Lesions

Coronary Stenosis

United States
Hillel Yaffe Medical Center

Unknown

Safety of Formalin-free Fixatives for In-Vivo Fixation of Skin Lesions.

Skin Abnormality

Israel
Boston Scientific Corporation

Completed

Randomized Trial Evaluating Slow-Release Formulation TAXUS Paclitaxel-Eluting Coronary Stent in the Treatment of In-Stent Restenosis (TAXUS V ISR)

Coronary Restenosis

United States, Canada
Anglo-European College of Chiropractic

Unknown

Massage of the Low Back Muscles Assessed With Ultrasound Scanning

Myofascial Pain Syndrome
Anglo-European College of Chiropractic

Completed

Effectiveness of a Massage Instrument Compared to Placebo for Upper Trapezius Muscle Pain

Myofascial Pain Syndrome

United Kingdom

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