Search clinical trials for: Premarin new tablet (fed)

Total 115 results

Pfizer

Completed

A Study To Compare The Amount Of Premarin Components That Is Absorbed Into The Blood Of Japanese Healthy Postmenopausal Women Following Oral Administration Of Two Different Tablets Of Premarin Under Fast and Fed Conditions.

Menopause | Vaginitis | Metrorrhagia | Primary Ovarian Insufficiency

Japan
Afeka, The Tel-Aviv Academic College of Engineering
Hebrew University of Jerusalem

Completed

Evaluation of Peripheral Microcirculation Hemodynamics Following Various Changes Based on Noninvasive Thermography (MRT02)

Microcirculation

Israel
Afeka, The Tel-Aviv Academic College of Engineering
Sheba Medical Center

Completed

Evaluating the State of Microvessels by Minimum Rise Time (MRT01) (MRT01)

Healthy

Israel
University of California, San Diego
National Eating Disorders Association

Enrolling by invitation

Outcomes of a Skill-Based Program for Eating Disorders (NEW FED TR)

Anorexia Nervosa

United States
Jiangsu HengRui Medicine Co., Ltd.

Active, not recruiting

A Relative Bioavailability Study of Different Processes of SHR2554 Tablets in Healthy Adult Subjects

Lymphoma

China
AstraZeneca

Completed

A Bioavailability Study Comparing 3 Different AZD1981 Tablets

Healthy

Sweden
GlaxoSmithKline

Completed

Relative Bioavailability and Food Effect Study for GSK163090 in Healthy Male and Female Volunteers

Depressive Disorder and Anxiety Disorders

Germany
Seoul National University Hospital

Withdrawn

Old Blood and Postoperative Complications

Postoperative Complications | Orthopedics | Red Blood Cells

Korea, Republic of
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Comparing Premarin® Vaginal Cream Versus Premarin® Oral Tablets in Atrophic Vaginitis

Atrophic Vaginitis

United States
Janssen Research & Development, LLC

Completed

Effect of Food on a Fixed Dose Combination Tablet of Canagliflozin and Metformin Immediate Release in Healthy Volunteers

Healthy
Centre for Global eHealth Innovation
University Health Network, Toronto; Trillium Health Partners

Unknown

Adoption, Acceptability, and Effectiveness of a Mobile Health App for Personalised Prostate Cancer Survivorship Care.

Prostate Cancer

Canada
GlaxoSmithKline

Completed

A Study to Assess the Relative Bioavailability of Different Formulations of GSK2018682, a Sphingosine-1-phosphate Receptor Subtype 1 Agonist, in Healthy Volunteers. (P1A114919)

Multiple Sclerosis, Relapsing-Remitting

Australia
AstraZeneca
Bristol-Myers Squibb

Completed

To Compare the Similarity of a Combination Dapagliflozin/Metformin Tablet With the Two Drugs Administered Separately

Type 2 Diabetes Mellitus

United Kingdom
Fujian Cancer Hospital

Not yet recruiting

New-mode Clinical Target Volume Delineation of Nasopharyngeal Carcinoma

Nasopharyngeal Carcinoma by AJCC V8 Stage
Paolo Cassano
North Suffolk Mental Health Association; Mclean Hospital

Completed

Transcranial Laser Therapy for Major Depressive Disorder (ELATED)

Major Depressive Disorder

United States
Galapagos NV

Completed

Oral Bioavailability of Two Solid Formulations of GLPG0634

Healthy

Belgium
Universidad Autonoma de Nuevo Leon
Hospital Universitario Dr. Jose E. Gonzalez

Recruiting

Binocular Visual Therapy and Video Games for Amblyopia Treatment.

Amblyopia

Mexico
Swiss Paraplegic Centre Nottwil
Swiss Federal Laboratories for Material Sciences and Technology

Completed

Low Friction Bed Sheet

Spinal Cord Injury | Pressure Ulcer

Switzerland
Galapagos NV
PRA Health Sciences

Completed

Bioavailability Study With GLPG1972

Osteoarthritis

Netherlands
Ferring Pharmaceuticals

Completed

A Phase III Study of FE 999913 in Japanese Female Patients Undergoing Fertility Treatment

Luteal Hormone Supplementation

Japan
Chuncheon Sacred Heart Hospital

Completed

Effects of Red Ginseng on Liver Function

Liver Dysfunction

Korea, Republic of
University of Manchester
City, University of London; Schepens Eye Research Institute

Terminated

Mobile Electronic Devices for Visual Impairment (MED4VI)

Vision, Low

United Kingdom
Sandoz

Completed

To Demonstrate the Relative Bioequivalence of Lisinopril 1 x 40 mg Tablet Under Fasting and Fed

Hypertension
Korea Ginseng Corporation
Nutrasource Pharmaceutical and Nutraceutical Services, Inc.

Recruiting

Effect of Korean Red Ginseng Extract on Blood Flow in Healthy Adults

Cardiovascular Diseases | Platelet Aggregation | Vasodilation | Blood Pressure Disorders

United States
University Health Network, Toronto
Queen Elizabeth II Health Sciences Centre; Rockyview General Hospital; Niagara... and other collaborators

Recruiting

Evaluating the Effectiveness of the Nurse Ned Clinic (NurseNed)

Prostate Cancer

Canada
Ablon Skin Institute Research Center
DeNova Research; Irish Response t/a Lifes2good

Completed

Efficacy of the New Viviscal Professional Strength Oral Supplement in Females With Thinning Hair

Hair Thinning
Pfizer

Recruiting

A Study for Two Tablet Forms of The Study Medicine (PF-07220060) in Healthy Adults

Healthy Participants

United States
Genentech, Inc.

Completed

Evaluation of the Relative Bioavailability and Food Effect of GDC-9545 in Healthy Females of Non-Childbearing Potential

Healthy Volunteers

United States
GlaxoSmithKline

Completed

A Study to Assess the Relative Bioavailability of Three Formulations and Food Effect on GSK1322322 in Healthy Subjects

Infections, Bacterial

United States
Hutchmed

Active, not recruiting

Human Mass Balance of [14C]HMPL-523 in Healthy Adult Male Chinese Subjects

Imumune Thrombocytopenia(ITP) Human Mass Balance

China
Pfizer

Completed

A Study to Investigate the Effect of Tablet Formulation and Food on PF-07104091 in Healthy Participants

Healthy

United States
Boehringer Ingelheim

Completed

Pharmacokinetics and Safety of BILR 355 in Healthy Male Volunteers

Healthy
Haukeland University Hospital
Vestre Viken Hospital Trust; Oslo University Hospital; University Hospital of... and other collaborators

Completed

Use of Blood and Plasma in Norwegian Physician-staffed Helicopter Emergency Medical System (ProHEMS)

Hemorrhagic Shock

Norway
Bayer

Completed

Relative Bioavailability and Food Effect Study With Vericiguat to Characterize the Pediatric Formulation in Adult Healthy Subjects

Pharmacokinetics

Germany
University Hospital of North Norway
The Research Council of Norway; European Commission; Oslo University College

Completed

Self-management in Type 2 Diabetes Patients Using the Few Touch Application

Type 2 Diabetes

Norway
Dr. J. Curtis Nickel
Stellar Pharmaceuticals

Completed

URACYST® For the Treatment of GAG Deficient Interstitial Cystitis

Interstitial Cystitis | Painful Bladder Syndrome

Canada
University Hospital, Bordeaux
Regional Health Agency New Aquitaine

Completed

Musitox® Project: Consumption of Psychoactive Substances at Music Festivals in Aquitaine (Musitox®)

Poisoning by Psychoactive Substances

France
Parc de Salut Mar

Completed

Analgesic Effect of Inhaled Lavender Essential Oil for Clipping of Tongue-ties (LEO-SME1)

Ankyloglossia

Spain
Sandoz

Completed

To Demonstrate the Relative Bioavailability Study of Loratadine 10 mg Tablets

Allergy
Hospitalsenheden Vest

Completed

Optimal Dietary Treatment of Obese Adults (OPDIOS)

Obesity | Overweight

Denmark
GlaxoSmithKline

Completed

A Study Assessing a Range of Formulations of the Fixed Dose Combination Product Containing Dutasteride (0.5mg) and Tamsulosin Hydrochloride (0.2mg) to Find a Formulation Which is Bioequivalent to Harnal-D Tablets (Tamsulosin Hydrochloride, 0.2mg) in Healthy Male Subjects From North East Asia

Prostatic Hyperplasia

Australia
Universidade do Porto
Center for Health Technology and Services Research; REQUIMTE/LAQV, Departamento... and other collaborators

Completed

Bioavailability of Red Wine Anthocyanins

Healthy

Portugal
Janssen Research & Development, LLC

Withdrawn

Study to Investigate the Food Effect and Oral Bioavailability of Tablet Formulations Relative to Suspension Formulation of JNJ-54416076 in Healthy Participants

Healthy

United States
Brigham and Women's Hospital
National Cancer Institute (NCI); Mayo Clinic; Albert Einstein College of Medicine and other collaborators

Completed

KEEPS Mammographic Density And Breast Health Ancillary Study (KEEPS MDBHAS)

Mammographic Density | Abnormal Mammogram

United States
Sandoz

Completed

To Demonstrate the Relative Bioavailability of Diclofenac Sodium 50 mg Enteric-Coated Tablets Under Non-Fasting Conditions

Inflammation
M.D. Anderson Cancer Center

Completed

Evaluation of the Anti-CD-33 Immunotoxin Hum-195/rGel in Patients With Advanced Myeloid Malignancies

Acute Myeloid Leukemia | Myeloproliferative Disorders | Chronic Myelomonocytic Leukemia | Anemia, Refractory, With Excess of Blasts

United States
Sandoz

Completed

To Demonstrate the Relative Bioavailability of Diclofenac Sodium 75 mg Enteric-Coated Tablets Under Non-Fasting Conditions

Inflammation
Akebia Therapeutics

Completed

Relative Bioavailability of Two Formulations of AKB-6548 and the Food Effect of a New Tablet in Healthy Adult Subjects

Healthy

United States
Mitsubishi Tanabe Pharma Corporation

Completed

The Confirmatory Study of TAU-284 in Pediatric Patients With Perennial Allergic Rhinitis

Perennial Allergic Rhinitis

Japan
Wageningen University
ADHD Research Centre

Completed

Biomarker Research in ADHD: the Impact of Nutrition (BRAIN)

Attention Deficit-Hyperactivity Disorder

Netherlands

Search clinical trials for: Premarin new tablet (fed)

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