Clinical Trials on Busulfan Pharmacokinetic Analysis

Total 3208 results

Mutual Pharmaceutical Company, Inc.

Completed

Drug-Drug Interaction Study of Colchicine and Theophylline

Pharmacokinetics

United States
Mutual Pharmaceutical Company, Inc.

Completed

Pharmacokinetic Study With Colchicine in Healthy Volunteers

Pharmacokinetics

United States
Mutual Pharmaceutical Company, Inc.

Completed

Drug-Drug Interaction Study Between Colchicine and Ketoconazole

Pharmacokinetics

United States
Mutual Pharmaceutical Company, Inc.

Completed

Drug-Drug Interaction Study of Colchicine and Clarithromycin

Pharmacokinetics

United States
Orion Corporation, Orion Pharma

Completed

Pharmacokinetic Study With Repeated Doses of Stalevo

Pharmacokinetics

Finland
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
CJ CheilJedang

Not yet recruiting

Pharmacokinetic Profile of Rosemary Extract Supplement

Pharmacokinetics
Il-Yang Pharm. Co., Ltd.

Recruiting

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

Pharmacokinetics

Korea, Republic of
Guangzhou General Hospital of Guangzhou Military...

Recruiting

Pharmacokinetics of Sugammadex in Reversal of Vecuronium-induced Neuromuscular Blockade in Patients During Laparoscopic Surgery

Pharmacokinetics

China
Guangzhou General Hospital of Guangzhou Military...
Guangdong Provincial Hospital of Traditional Chinese Medicine

Recruiting

Pharmacokinetics of Sugammadex for the Reversal of Moderate Neuromuscular Blockade in Patients During Renal Transplantation

Pharmacokinetics

China
Guangdong Raynovent Biotech Co., Ltd

Completed

Mass Balance Study of [14C]RAY1216 in Healthy Adult Male Subjects in China

Pharmacokinetics

China
Ascentage Pharma Group Inc.

Completed

The Absorption, Metabolism and Excretion of [14C]APG-2575 in Healthy Subjects

Pharmacokinetics

China
Factors Group of Nutritional Companies Inc.

Completed

Comparing the Pharmacological Profile of Formulations Containing Omega 3 Fatty Acids

Pharmacokinetics

Canada
BHB Therapeutics, Ireland LTD
Mérieux NutriSciences Biofortis

Completed

Pharmacokinetics of Two Fatty Acid Ketone Esters

Pharmacokinetics

United States
Factors Group of Nutritional Companies Inc.

Completed

Pharmacological Profile of Different Berberine Formulations, and Effects on Blood Sugar Levels

Pharmacokinetics

Canada
NeuroSense Therapeutics Ltd.

Completed

A Multiple-Dose PK Study to Evaluate the Comparative Bioavailability of PrimeC Tablets to Ciprofloxacin Tablets Co-administered With Celecoxib Capsules, in Healthy Adult Subject

Pharmacokinetics

United States
University of Utah
Center for Addiction and Mental Health

Active, not recruiting

Pharmacokinetics of Amiloride Nasal Spray in Healthy Volunteers

Pharmacokinetics

United States
NeuroSense Therapeutics Ltd.

Completed

A Pilot Study to Evaluate the PK Profile of PrimeC-ER Tablets in Healthy Adult Subjects

Pharmacokinetics

United States
Nanjing Yoko Biomedical Co., Ltd.

Completed

Study on Tolerance, Pharmacokinetics and Drug Interaction of YK-1169 in Healthy Volunteers

Pharmacokinetics

China
Bayer

Completed

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

Pharmacokinetics

Germany
Joint Stock Company "Farmak"

Completed

Fasting Bioequivalence Study of 2 Progesterone Soft Capsules 200 mg in 66 Healthy Female Subjects Under Vaginal Route

Pharmacokinetics

Jordan
Joint Stock Company "Farmak"

Completed

Fasted Bioequivalence Study of 2 Olanzapine Film-coated Tablets, 5 mg, in Healthy, Adult Male and Female Subjects.

Pharmacokinetics

Czechia
Teva Branded Pharmaceutical Products R&D, Inc.

Completed

A Pharmacokinetic Study to Evaluate the Bioequivalence of 2 Progesterone Vaginal Rings in Postmenopausal Women

Pharmacokinetics

United States
Teva Branded Pharmaceutical Products R&D, Inc.

Completed

Study to Characterize the Pharmacokinetics and Safety of TV-45070 Ointment in Healthy Volunteers

Pharmacokinetics

United States
Amgen

Completed

Study to Evaluate the Pharmacokinetics of Single and Multiple Doses of Apremilast in Healthy Adult Male Korean Subjects

Pharmacokinetics

Korea, Republic of
Pfizer

Withdrawn

A SINGLE-DOSE, 2-ARM, PHARMACOKINETIC STUDY OF PF-06439535 (CN) AND EUROPEAN UNION SOURCED BEVACIZUMAB IN CHINESE HEALTHY MALE VOLUNTEERS

Pharmacokinetics

China
Scynexis, Inc.
Clinical Network Services (CNS) Pty Ltd

Completed

Study to Evaluate the Effect of SCY-078 (Ibrexafungerp) on the PK of Pravastatin in Healthy Subjects

Pharmacokinetics

Australia
Pharmaxis

Completed

A Two-part Pharmacokinetic Study of PXS-5382A in Healthy Adult Males

Pharmacokinetics

Australia
Daiichi Sankyo, Inc.

Completed

A Study to Determine the Effects of Itraconazole on the Pharmacokinetics (PK) of DS-8500 in Healthy Subjects

Pharmacokinetics

United States
Grünenthal GmbH
Grünenthal Colombiana S.A.

Completed

Administration of Tramadol and Ketorolac Separately and Simultaneously to Assess a Potential Pharmacokinetic Interaction

Pharmacokinetics

Mexico
Merck Sharp & Dohme LLC

Completed

A Single Dose Study of the Safety, Pharmacokinetics and Pharmacodynamics of MK-1064 (MK-1064-001)

Pharmacokinetics
Université de Montréal

Unknown

Kinetic Time Courses of Bisphenol-S in Volunteers

PHARMACOKINETICS

Canada
Boston Medical Center

Completed

The Pharmacokinetics of 12 Week Continuous Patch Use

Pharmacokinetics

United States
Seoul National University Hospital

Completed

A Randomized, Open-label, Two-way Crossover Study to Assess the Pharmacokinetics and Safety of CK-30 600 mg (Compound K)

Pharmacokinetics

Korea, Republic of
AcelRx Pharmaceuticals, Inc.

Completed

Effect of Ketoconazole on Sufentanil NanoTab Pharmacokinetics

Pharmacokinetics

United States
Celgene Corporation

Completed

Study to Evaluate the Effect of Cytochrome P450 (CYP) 3A Inhibition and Induction on the Pharmacokinetics of CC-220 in Healthy Subjects

Pharmacokinetics

United States
University of Florida

Completed

The Effect of Low Furanocoumarin Grapefruit Hybrid Juice Consumption on Midazolam Pharmacokinetics

Pharmacokinetics

United States
H. Lundbeck A/S

Completed

Pharmacokinetic Properties of Vortioxetine in Healthy Young Chinese Men and Women

Pharmacokinetics

China
Oxford Pharmascience Ltd

Completed

Phase I Study PK Study With OXP005 and Naprosyn

Pharmacokinetics

United Kingdom
Alkermes, Inc.

Completed

A Drug-Drug Interaction Study of ALKS 5461 in Healthy Volunteers

Pharmacokinetics

United States
Repros Therapeutics Inc.

Completed

An Open-Label Study to Evaluate the Effect of Age Upon the Pharmacokinetics of Androxal

Pharmacokinetics

United States
Bayer

Completed

Pharmacokinetic Study Comparing Aspirin and Effervescent Aspirin

Pharmacokinetics

United States
Bayer

Completed

Pharmacokinetics Study Comparing Naproxen Sodium Extended Release and Naprelan

Pharmacokinetics

United States
Bayer

Completed

Pharmacokinetic Study Comparing Aspirin and Aspirin Granules

Pharmacokinetics

United States
UCB Pharma

Completed

The First Clinical Study to Test Safety, Blood Levels and Other Effects of CDP6038 in Healthy Males

Pharmacokinetics

Germany
Sunovion

Completed

A Randomized, Placebo-Controlled, Two-Period, Crossover Study to Evaluate the Effect of Lurasidone HCl on Oral Contraceptive Pharmacokinetics in Healthy Female Subjects (OC-DDI)

Pharmacokinetics

United States
AstraZeneca

Completed

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

Pharmakokinetic

Sweden
AstraZeneca

Completed

An Open-Label, Single and Multiple Dose Pharmacokinetic Study of 90 mg and 180 mg Doses of AZD6140 in Healthy Volunteers

Pharmacokinetics

China
Photocure

Completed

An Open-label, Single-dose, Three Period Study to Determine the Pharmacokinetic Parameters of Hexaminolevulinate (HAL) Hydrochloride After Vaginal, Enema and Intravenous Administration of Healthy Female Volunteers

Pharmacokinetics

Netherlands

3

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