Search clinical trials for: Reference formulation

Total 1973 results

Gesynta Pharma AB
CTC Clinical Trial Consultants AB; RISE Research Institutes of Sweden AB

Completed

A Study in Healthy Subjects to Evaluate Pharmacokinetics and Food Effect After Dosing of GS-248

Pharmacokinetic

Sweden
Lund University

Completed

Effects of Whole Grain Rye on Metabolic Risk Markers and Mood

Metabolic Disorders and Cognitive Decline
Leo Wang
West China Hospital

Completed

Clinical Trial of Transtek Body Fat Analyzer (GBF-835-N2 & Other 7 Models) (15001Analy)

Weight | Body Fat Disorder

China
University Hospital, Grenoble

Completed

a Randomized Multicenter Trial Comparing Vacuum Assisted Delivery With the New Device "iCUP" Versus the Reference Cup. (ICUP)

Randomized Controlled Trials | Vacuum Extraction, Obstetrical | Failures, Medical Device | Maternal Lesions | Neonatal Lesions

France
AstraZeneca

Completed

Single Dose Study to Assess Efficacy and Safety of 4 Doses of LAS100977 in Chronic Obstructive Pulmonary Disease (COPD) Population

Chronic Obstructive Pulmonary Disease (COPD)

Germany
Karolinska Institutet

Active, not recruiting

Live Supervision in Psychotherapy: Study Protocol for a Single Case Experimental Design Study (SCED)

Competence

Sweden
Pfizer

Completed

OPEN LABEL, 2-PERIOD STUDY, TO COMPARE BIO-AVAILABILITY OF 2 DIFFERENT FORMULATIONS OF PF-05221304 IN HEALTHY ADULTS

Healthy

United States
HK inno.N Corporation

Completed

A Study to Compare the Pharmacokinetic Characteristics of CJ-12420

Erosive Esophagitis

Korea, Republic of
Eli Lilly and Company

Completed

A Research Study Looking at Similarity Between LY3437943 Versions for Different Injection Devices

Healthy

United States
GlaxoSmithKline

Completed

A Study to Evaluate the Safety, Reactogenicity and Immunogenicity of GSK Biologicals' Non-typeable Haemophilus Influenzae (NTHi) Investigational Vaccine (GSK2838497A) in Current and Former Smokers

Respiratory Disorders

Belgium
Boehringer Ingelheim

Not yet recruiting

A Study in Healthy People to Compare How 2 Different High Dose Formulations of BI 1015550 Are Taken up in the Body

Healthy
Allergan

Completed

Safety and Efficacy of AGN-210961 Ophthalmic Solution Compared With Bimatoprost Ophthalmic Solution in Patients With Glaucoma or Ocular Hypertension

Ocular Hypertension | Primary Open-Angle Glaucoma

United States
Hoffmann-La Roche

Completed

A Bioequivalence Study of Pegylated Interferon Alfa-2a (PEG-IFN Alfa-2a) Benzyl Alcohol (BA)-Free Formulation Versus PEG-IFN Alfa-2a (Pegasys) Following Subcutaneous Administration

Healthy Volunteers

New Zealand, Taiwan, Australia, Hong Kong, Singapore
Ansun Biopharma, Inc.

Completed

Phase 2B Study on Safety and Therapeutic Efficacy of DAS181 in Adult Subjects With Naturally Acquired Influenza

Influenza

United States
Eli Lilly and Company

Completed

A Study of LY3039478 in Healthy Participants

Healthy

United States
Merck Sharp & Dohme LLC

Completed

Bioequivalence of Two Tablet Forms of MK0974 (0974-045)

Migraine
GlaxoSmithKline

Active, not recruiting

Safety, Efficacy, Immunogenicity Study of GSK Biologicals' HBV Viral Vector and Adjuvanted Proteins Vaccine (GSK3528869A) in Adult Patients With Chronic Hepatitis B Infection

Hepatitis B, Chronic

Taiwan, Belgium, Thailand, Germany, Spain, Hong Kong, United Kingdom, France, Poland
Pfizer

Completed

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

Healthy

United States
JW Pharmaceutical

Completed

To Evaluate the Safety and PK Characteristics in Healthy Volunteers

Healthy

Korea, Republic of
Padagis LLC

Completed

To Compare Safety and Efficacy of Perrigo's Drug Product Compared to an FDA Approved Drug Product in the Treatment of Actinic Keratosis

Actinic Keratosis
Allergan

Completed

Safety and Tolerability of AGN-199201 in Patients With Erythema Associated With Rosacea

Erythema | Rosacea

United States
Forendo Pharma Ltd
Richmond Pharmacology Limited

Completed

A Relative Bioavailability Study of FOR-6219 in Capsule and Tablet Formulations

Relative Bioavailability

United Kingdom
Repros Therapeutics Inc.

Completed

Comparison of Two Formulations of Proellex for Vaginal Administration

Comparison of 2 Different Formulations of 12 mg Proellex Vaginal Capsules

United States
Dexa Medica Group

Completed

Bioequivalence Evaluation of Two Film-Coated Formulations of Valsartan 160 mg

Healthy

Indonesia
Korea United Pharm. Inc.

Not yet recruiting

A Study to Compare and Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of UI059 and UIC202201

Gastro-Intestinal Disorder

Korea, Republic of
Hamilton Health Sciences Corporation

Recruiting

Rapid POC GAS Diagnostics in the Paediatric ED

Streptococcal Pharyngitis

Canada
Korea United Pharm. Inc.

Completed

A Study to Compare Pharmacokinetics, Pharmacodynamics and Safety of UI059 and UIC202201 in Healthy Subjects

GERD

Korea, Republic of
Darma Inc.
Medstar Health Research Institute

Completed

Pilot Clinical Evaluation of the RHEA Vital Sign Vigilance System in Hospital Patients Patients

Vital Sign Monitoring

United States
Darma Inc.
Tufts Medical Center

Completed

Pilot Clinical Evaluation of the RHEA Vital Sign Vigilance System in Hospital Patients

Vital Sign Monitoring

United States
Beckman Coulter, Inc.

Completed

DxH520 Pediatric Reference Interval Verification

Healthy Subjects

Canada
Assistance Publique - Hôpitaux de Paris

Recruiting

Evaluation of the Metrological Reliability of Connected Objects in the Measurement of Medical Physiological Parameters (EVALEXPLO)

Respiratory; Disorder, Functional, Impaired

France
Beth Israel Deaconess Medical Center
Brigham and Women's Hospital

Active, not recruiting

Utility of Cortical Bone Tissue Properties in the Assessment of Fracture Risk

Hip Fractures | Osteoporosis | Distal Radius Fracture

United States
Léman Micro Devices SA

Withdrawn

A Study to Demonstrate the Clinical Accuracy of the Smartphone Vital Signs System (SVSS)

Healthy Volunteers

Switzerland
University of North Carolina, Chapel Hill
National Institutes of Health (NIH)

Terminated

Safety Study of 20,000 EU of Clinical Center Reference Endotoxin in Allergic Adults With and Without Mild Asthma

Mild Allergic Rhinitis | Mild Allergic Rhinitis With Mild Asthma

United States
King's College London

Completed

Pharmacokinetic Study of a Novel Lipid Formulation of Cannabidiol Compared to a Standard Formulation (CLIP)

Absorption; Chemicals

United Kingdom
Padagis LLC

Completed

To Compare Safety and Efficacy of Perrigo's Drug Compared to an FDA Approved Drug in the Treatment of Actinic Keratosis

Actinic Keratosis
Örebro University, Sweden

Not yet recruiting

Effects of In-between Meal Products on Cognitive Function in Older Adults (Minimeal)

Cognitive Function
University Hospital, Toulouse

Completed

Assessment of the New Automated Vitrification System "GAVI" for Early Cleaved Embryos Cryopreservation (GAVI)

Fertility Disorders

France
Poxel SA

Completed

Bioequivalence of Imeglimin Tablet Formulations

Bioequivalence

United Kingdom
University of Paris 13
Intitut National du Cancer

Completed

Online Experimental Supermarket (SUPERNET)

Food Selection

France
University of North Carolina, Chapel Hill
National Institute of Environmental Health Sciences (NIEHS)

Completed

Inhalation of 20,000 Endotoxin Units(EU) of Clinical Center Reference Endotoxin in Healthy Volunteers (Entox)

Healthy Adults

United States
Imperial Brands PLC
Nerudia Ltd

Completed

An Exploratory PET-study of Deposition, Disposition and Brain Uptake of [11C]Nicotine After Inhalation of 2 Nicotine Formulations Via the myBluTM E-cigarette in Smokers

Healthy Volunteers

Sweden
AbbVie

Completed

Study to Assess Adverse Events and Compare How Two Subcutaneous ABBV-154 Injection Formulations Move Through the Body of Adult Healthy Participants

ABBV-154

United States
Chong Kun Dang Pharmaceutical

Completed

Exploratory Trial to Evaluate the Pharmacokinetic Properties and Safety of CKD-828 in Healthy Subjects

Hypertension

Korea, Republic of
Atea Pharmaceuticals, Inc.
Hoffmann-La Roche

Completed

Study of AT-527 in Healthy Subjects (R07496998)

Healthy Volunteer Study

Canada
MedImmune LLC

Completed

A Pilot Study Investigating Bioequivalence Between a Single Dose of Formulation 2 and Formulation 3 of MEDI0382

Type 2 Diabetes Mellitus

United States
GlaxoSmithKline

Completed

Study to Evaluate the Safety, Reactogenicity and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Investigational Respiratory Syncytial Virus (RSV) Vaccines

Infections, Respiratory Syncytial Virus

Canada
Otsuka Australia Pharmaceutical Pty Ltd

Completed

Refine and Assess the Readability of Patient, Carer, and Clinician Treatment Preference in Myelodysplasia Questionnaire (TPMQ)

Myelodysplastic Syndrome (MDS)

Australia
The Affiliated Hospital of Qingdao University
Changzhou Pharmaceutical Factory Co., Ltd

Not yet recruiting

Bioequivalence Study of Ezetimibe Tablets Under Fasting Conditions in Healthy Subjects

Pharmacokinetics | Safety
Indonesia University
PT Paragon Technology and Innovation

Completed

Sun Protection Factor (SPF) / UVA Protection Factor Study

Sunscreen Agents

Indonesia

3

Subscribe