Clinical Trials on Pharmacokinetics of ASP1707

Total 27139 results

Hartford Hospital
Shionogi Inc.

Active, not recruiting

Cefiderocol Plasma Concentrations in Patients Receiving Renal Replacement Therapy

Pharmacokinetics

United States
Yiling Pharmaceutical Inc.

Completed

A Phase I Pharmacokinetics Study for KT07 Capsule

Pharmacokinetics | Healthy Adult Subjects | Safety and Tolerability

United States
Joint Stock Company "Farmak"

Completed

Fed Bioequivalence Study of 2 Metformin 1000 mg Prolonged Release Tablets in 28 Healthy Male and Female Volunteers

Pharmacokinetics

Czechia
Daiichi Sankyo Co., Ltd.

Completed

A Study of the Effect of Quizartinib on the Pharmacokinetics of the P-gp Substrate Dabigatran Etexilate in Healthy Participants

Healthy Subjects | Pharmacokinetics | Drug-drug Interaction | Quizartinib

United States
Astellas Pharma Europe B.V.

Completed

Study to Evaluate the Effect of Solifenacin and Mirabegron on the Tamsulosin Hydrochloride (HCl) Concentrations in Blood in Healthy Male Subjects

Healthy Subjects | Pharmacokinetics | Drug-Drug Interaction (DDI)

Germany
University of North Carolina, Chapel Hill

Completed

Pharmacokinetic Study of Raltegravir in Healthy Premenopausal Women.

Pharmacokinetics

United States
Abbott Products
Quintiles, Inc.

Terminated

First in Man Study With SLV342

Pharmacokinetics

United Kingdom
University of Washington
Oregon Health and Science University; National Institute of General Medical...

Unknown

Naproxen Pharmacogenetic Study (Project 1, Aim 2)

Pharmacogenetics

United States
University of British Columbia
GlaxoSmithKline; Merck Sharp & Dohme LLC; Pfizer; Roche Pharma AG; AstraZeneca; Janssen... and other collaborators

Completed

The Implementation of Pharmacogenomics Into Primary Care in British Columbia (IPPC)

Pharmacogenetics
Universidad Peruana Cayetano Heredia

Completed

Pharmacokinetics of Diammine Silver Fluoride

Fluoride and Silver Pharmacokinetics of DSF Applied Topically to Teeth of Adults. Erythema, Bleeding, White Changes, Ulceration and Pigmentation Were Assessed

Peru
Aker Biomarine Antarctic AS
BioTeSys GmbH

Completed

Uptake of an Omega-3 Oil in Healthy Adults

Pharmacokinetics | Absorption

Germany
Cui Yimin

Unknown

Impact of Biomarkers on Pharmacokinetics and Pharmacodynamics of Ticagrelor

Pharmacokinetics | Pharmacodynamics | Pharmacogenomics | Accurate Medication | Ticagrelor

China
University Medicine Greifswald

Completed

Oral Pharmacokinetics of Sulfasalazine, Paracetamol, Fexofenadine and Valsartan Using Different Administration Mediums

Pharmacokinetics | Magnetic Resonance Imaging | Administration, Oral
Bausch & Lomb Incorporated

Completed

Tear Fluid Levels of Loteprednol Etabonate Ophthalmic Gel 0.5% Following a Single Instillation

Pharmacokinetics

United States
King Faisal Specialist Hospital & Research Center

Completed

The Placebo Effect May Involve Modulating Drug Bioavailability

Pharmacokinetics | Placebo Effect | Drug Half Life

Saudi Arabia
Johnson & Johnson Pharmaceutical Research & Development...

Completed

Bioequivalence Study of the Oral Contraceptive Tablet Containing Norgestimate (NGM)/Ethinyl Estradiol (EE) With or Without Folic Acid in Healthy Women.

Female Contraception | Contraception | Pharmacokinetics | Therapeutic Equivalency
University of Oxford
Mahidol University; Mahidol Oxford Tropical Medicine Research Unit

Recruiting

Pharmacokinetic Study of Artemether-lumefantrine and Amodiaquine in Healthy Subjects (ALAQ)

Healthy | Pharmacokinetic | Drug Combination

Thailand
Everstar Medicines (Shanghai) Limited

Completed

A Study of Ralinepag in Healthy Chinese Adult Subjects

Healthy Volunteer | Pharmacokinetic Study

China
Joanneum Research Forschungsgesellschaft mbH

Completed

An Exploratory Study in Healthy Volunteers to Identify Factors Influencing Bioequivalence Studies on Moderately Lipophilic Drugs Using Dermal Open Flow Microperfusion (dOFM)

Healthy | Dermal Pharmacokinetic Measurements

Austria
Samuel Fortin

Completed

Effect of Fish Oil Monoglycerides on the Omega-3 Index

Pharmacokinetic in Normal Population

Canada
HK inno.N Corporation

Completed

To Investigate PK and PD of CJ-12420, Clarithromycin, Amoxicillin After Multiple Dose Administration

Drug Interaction | Pharmacokinetic | Pharmacodynamic

Korea, Republic of
AstraZeneca

Completed

Explore the Performance of IntelliCap.

Pharmacokinetic Profile | Plasma Concentration

United Kingdom
University Hospital, Limoges

Completed

Pharmacokinetic Study of Adoport® (Tacrolimus) in Patients With de Novo Kidney Transplantation (IMPAKT)

Transplantation | Pharmacokinetic | Kidney

France
Pharmaceutical Productions Inc.
National Institute on Drug Abuse (NIDA)

Completed

Pilot Pharmacokinetic Study of Investigational Sublingual Nicotine Tablet Versus COMMIT Nicotine Lozenge

Nicotine Pharmacokinetic Study

United States
Il-Yang Pharm. Co., Ltd.

Not yet recruiting

Study to Evaluate the Safety and the Pharmacokinetics of IY-NT-T

Pharmacokinetics

Korea, Republic of
Joint Stock Company "Farmak"

Completed

Fed Bioequivalence Study of 2 Metformin 500 mg Prolongued Release Tablets in 28 Healthy Male and Female Volunteers

Pharmacokinetics

Czechia
Walter Reed Army Institute of Research (WRAIR)

Withdrawn

Malarone Pharmacokinetics Under Simulated Physiologic Stressors of Deployment (MPUSPSD)

Exercise | Pharmacokinetics

United States
Royal Brisbane and Women's Hospital
The University of Queensland

Completed

Pharmacokinetics of Ceftolozane/Tazobactam in Plasma and Cerebrospinal Fluid

Pharmacokinetics

Australia
Celgene

Completed

A Phase 1 Open-Label Study to Evaluate the Metabolism and Excretion of CC-223 and the Effect of Food on the Pharmacokinetics of CC-223 in Healthy Male Adult Subjects (AME/FE)

Safety and Pharmacokinetics in Healthy Volunteer Subjects

United States
Astellas Pharma Europe B.V.

Completed

Study to Evaluate the Effect of Solifenacin and Mirabegron on the Digoxin Concentrations in Blood in Healthy Subjects

Healthy Subjects | Pharmacokinetics | Drug-Drug Interaction (DDI)

Germany
Bayer

Completed

The Effect of Food (High Fat and Low Fat Breakfast) on the Pharmacokinetics of Regorafenib

Pharmacokinetics | Dietary Fats

United States
University Hospital Birmingham NHS Foundation Trust

Completed

Blood Propofol Measurement During Anaesthesia Using Propofol Target Controlled Infusion

Pharmacokinetics | General Anaesthesia | Propofol | Target Controlled Infusion

United Kingdom
Tris Pharma, Inc.
Forest Laboratories

Completed

Evaluation of the Effects of Multiple Doses of Cebranopadol on the Electrical Activity of the Heart in Healthy Subjects

Prolonged QTc Interval | Pharmacokinetic

United States
University of Oxford
Mahidol University; Mahidol Oxford Tropical Medicine Research Unit

Terminated

Study of Artemether-lumefantrine, Amodiaquine and Primaquine in Healthy Subjects (ALAQPQ)

Healthy | Pharmacokinetic | Drug Combination

Thailand
Astellas Pharma Global Development, Inc.

Completed

A Dose Escalation Study to Assess Safety, Tolerability and Pharmacokinetics of ASP2409 Following a Single Intravenous Dose in Patients With Rheumatoid Arthritis on Methotrexate

Rheumatoid Arthritis | Pharmacokinetics of ASP2409

United States
Astellas Pharma Global Development, Inc.

Completed

A Study To Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of ASP2408 After Multiple Dose Subcutaneous Injections in Patients With Rheumatoid Arthritis on Methotrexate

Rheumatoid Arthritis | Pharmacokinetics of ASP2408

United States
AstraZeneca

Completed

A Drug-Drug Interaction Study to Study the Effect of AZD1981 on Warfarin

Pharmakokinetic

Sweden
Amphastar Pharmaceuticals, Inc.

Completed

Comparison of the Pharmacokinetics (PK) and Pharmacodynamics (PD) Biosimilarity of Proposed Biosimilar Rapid-Acting Insulin Aspart (I004) and NovoLog After Single-Dose Subcutaneous Administration to Healthy Volunteers

Pharmacokinetics | Pharmacodynamics

United States
Hospital Clinic of Barcelona
University of Barcelona

Completed

Pharmacokinetic Model of Fibrinogen Plasma Levels After Fibrinogen Administration (PKMF)

Fibrinogen; Deficiency, Acquired | PHARMACOKINETICS

Spain
Pfizer

Completed

Evaluating QTc, PK, Safety of Gemtuzumab Ozogamicin (GO) in Patients With CD33+ R/R AML

Pharmacokinetics | Safety | ECG

Canada, Spain, United States, Hungary, Poland, United Kingdom
Biolab Sanus Farmaceutica

Withdrawn

Pharmacokinetics Trial of Isosorbide Mononitrate 0.5% Gel for Intra Anal Application in Healthy Subjects

Healthy Subjects | Pharmacokinetics
National Institute of Mental Health (NIMH)

Completed

Evaluation of a Novel PET Radioligand to Image OGA

Pharmacokinetics | Adult

United States
University of Hohenheim

Completed

Comparison of Curcumin Bioavailability

Safety After Oral Intake | Pharmacokinetics After Oral Intake

Germany
University of Hohenheim

Completed

Bioavailability of Resveratrol From Vineatrol30 Extract Incorporated Into Micelles

Safety After Oral Intake | Pharmacokinetics After Oral Intake

Germany
Duke University
National Institute of General Medical Sciences (NIGMS)

Completed

Delivery of Pharmacogenetic Testing in a Community Pharmacy Setting

Pharmacogenetics

United States
Geropharm

Recruiting

Double-blind, Randomized Comparative Cross-sectional Study of Pharmacodynamics and Pharmacokinetics of Drugs GP40141

Pharmacokinetics | Pharmacodynamics | Bioequivalence

Russian Federation
Cinclus Pharma AG

Recruiting

A Study to Investigate the Pharmacokinetics and ECG Effects of Linaprazan Glurate

GERD | Pharmacokinetics | Cardiodynamic ECG | Safety, and Tolerability

Sweden
Daiichi Sankyo Co., Ltd.

Completed

A Study of the Effect of a Moderate CYP3A Inducer Efavirenz on Quizartinib Pharmacokinetics in Healthy Participants

Healthy Subjects | Pharmacokinetics | Drug-drug Interaction | Quizartinib

United States
University of Florida
National Center for Complementary and Integrative Health (NCCIH); Thorne Research...

Completed

A Phased Clinical Trial of Dietary Supplemental Kava: Kava Pharmacokinetics (Kava PK)

Pharmacokinetics

United States
Food and Drug Administration (FDA)
Spaulding Clinical Research LLC

Completed

Clinical Study to Investigate the Urinary Excretion of N-nitrosodimethylamine (NDMA) After Ranitidine Administration

Pharmacokinetics | Food-drug Interaction | Ranitidine Adverse Reaction

United States

Clinical Trials on Pharmacokinetics of ASP1707

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Bangladesh

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations