Search clinical trials for: Therapeutic Equivalency

Total 12347 results

Cao Yu

Recruiting

Bioequivalence of Ezetimibe Tablets in Healthy Subjects

Therapeutic Equivalency

China
Mylan Pharmaceuticals Inc
Genpharm ULC

Completed

Fed, Bioequivalence Study of Pravastatin Sodium 80 mg Tablets Versus Pravachol® 80 mg Tablets In Subjects

Therapeutic Equivalency

Canada
Mylan Pharmaceuticals Inc
Genpharm ULC

Completed

Fasting Bioequivalence Study of Pravastatin Sodium 80 mg Tablets Versus Pravachol® 80 mg Tablets In Normal Healthy Subjects

Therapeutic Equivalency

Canada
Geropharm

Completed

Comparative Study of Rinsulin R (GEROPHARM) and Humulin Regular (Eli Lilly) Euglycemic Hyperinsulinemic Clamp Method

Bioequivalence | Therapeutic Equivalency

Russian Federation
The Affiliated Hospital of Qingdao University

Completed

Bioequivalence Study of Two Irbesartan in Healthy Chinese Subjects

Therapeutic Equivalency

China
Laboratorios Andromaco S.A.

Completed

Bioavailability of Levonorgestrel and Ethinyl Estradiol Tablets 15.0 mg/0.03 mg With Regards to Reference Product

Therapeutic Equivalency

India
Orphelia Pharma

Completed

Bioequivalence Study Between Temozolomide Oral Suspension (Ped-TMZ) and Temodal® Capsules

Therapeutic Equivalency

France
The Affiliated Hospital of Qingdao University

Completed

A Randomized Phase 1 Study of Liralutide Injection in Healthy Chinese Subjects

Therapeutic Equivalency

China
Nova Laboratories Limited
Syne Qua Non Limited; Medicines Evaluation Unit Ltd; Alderley Analytical Ltd; Black... and other collaborators

Completed

Bioequivalence of Azathioprine Suspension 10 mg/mL (Jayempi) Versus Azathioprine Tablet 50mg (Imurek®) (AZA)

Therapeutic Equivalency

United Kingdom
University of Maryland, Baltimore
Food and Drug Administration (FDA)

Completed

Transdermal Patch CVD 1000: The Effect of Heat on Nicotine Release From Nicotine Patches in Adult Smokers

Smoking

United States
The Affiliated Hospital of Qingdao University

Completed

Bioequivalence Evaluation of Two Fixed-dose Combination of Lisinopril 10mg/Levamlodipine Besylate 5mg in Healthy Chinese Subjects

Therapeutic Equivalency

China
Cao Yu

Unknown

Bioequivalence of Extended Release Nifedipine Tablets in Healthy Chinese Subjects

Therapeutic Equivalency

China
Orphelia Pharma

Completed

Bioequivalence Study of Vigabatrin ORPHELIA Pharma 500mg Soluble Tablets and SabrilTM 500mg Granules for Oral Administration

Therapeutic Equivalency

France
University of Maryland, Baltimore
Food and Drug Administration (FDA)

Completed

Fentanyl Patch Pharmacokinetics in Healthy Adults

Peer Review, Research

United States
University of Maryland, Baltimore
Food and Drug Administration (FDA)

Completed

Transdermal Patch CVD 2000: The Effect of Heat on Fentanyl Release From Fentanyl TDSs in Healthy Adults

Peer Review, Research

United States
Mahidol University

Completed

Generic Substitution of Original Levetiracetam in Thai Epilepsy Patients

Epilepsy

Thailand
Luis Eduardo Morales Buenrostro

Completed

Pharmacokinetic Parameters of Innovative Valganciclovir Versus Generic Valganciclovir

Kidney Transplantation | Pharmacokinetics | Cytomegalovirus Infections | Therapeutic Equivalency

Mexico
Pfizer

Withdrawn

A Bioequivalence Study Comparing Methylprednisolone Suspension to Methylprednisolone Tablets Under Fed Conditions

Therapeutic Equivalency
Pfizer

Withdrawn

A Bioequivalence Study Comparing Methylprednisolone Suspension To Methylprednisolone Tablets

Therapeutic Equivalency
Pfizer

Withdrawn

A Bioequivalence Study Comparing Methylprednisolone Suspension To Methylprednisolone Tablets Under Fasting Conditions

Therapeutic Equivalency
Federal University of São Paulo
Fundação de Amparo à Pesquisa do Estado de São Paulo

Completed

Therapeutic Equivalence Between Branded and Generic WARFArin Tablets in Brazil (WARFA)

Atrial Fibrillation

Brazil
National Heart, Lung, and Blood Institute (NHLBI)

Completed

Beta-Blocker Evaluation in Survival Trial (BEST)

Heart Diseases | Cardiovascular Diseases | Heart Failure | Heart Failure, Congestive
Bayer
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

Completed

Bioequivalence Study in Healthy Subjects, 2*5 mg Tablets Rivaroxaban Versus 1*10 mg Tablet Rivaroxaban

Therapeutic Equivalency

Germany
National Cancer Institute (NCI)

Completed

Edrecolomab in Treating Patients With Stage II Colon Cancer

Mucinous Adenocarcinoma of the Colon | Signet Ring Adenocarcinoma of the Colon | Stage IIA Colon Cancer | Stage IIB Colon Cancer | Stage IIC Colon Cancer

United States
Mutual Pharmaceutical Company, Inc.

Completed

Fasted Pharmacokinetic and Bioequivalency Study of Fenofibric Acid

Healthy
Mutual Pharmaceutical Company, Inc.

Completed

Bioequivalence Study of Zolpidem Tartrate Tablets and Ambien® Under Fasting Conditions

Healthy
Pfizer

Completed

A Study To Determine Bioequivalence Between The Commercial Femulen Tablets And A Reformulation Of Femulen Tablets In Healthy Female Subjects

Therapeutic Equivalency

Singapore
Johnson & Johnson Consumer and Personal Products...

Completed

Ivermectin Solution Bioequivalence Study - Fasted

Healthy

Ireland
Johnson & Johnson Consumer and Personal Products...

Completed

Ivermectin Solution Bioequivalence Study - With Food (Repeat)

Healthy
Johnson & Johnson Consumer and Personal Products...

Completed

Ivermectin Solution Bioequivalence Study - With Food

Healthy
University of Ottawa

Unknown

Comparison of the Pharmacokinetics of Three Generic Medications and Their Respective Brand Preparations

Healthy

Canada
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
Johnson & Johnson Pharmaceutical Research & Development...

Completed

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

Pharmacokinetics | Therapeutic Equivalency | Contraceptives, Oral
Mutual Pharmaceutical Company, Inc.

Completed

Fed Bioequivalence Study of Zolpidem Tartrate Tablets and Ambien® Tablets

Healthy | Therapeutic Equivalency
Bristol-Myers Squibb

Completed

A Study Comparing Two Forms of Didanosine in HIV-infected Patients

HIV Infections
Pfizer

Completed

Phase1, Single Dose, Crossover Study to Determine Bioequivalence

Healthy

Singapore
Pfizer

Completed

Phase 1, Single Dose, Crossover Study to Determine Bioequivalence and to Investigate Food Effect

Food | Therapeutic Equivalency

Japan
Mutual Pharmaceutical Company, Inc.

Completed

Fed Bioavailability Study of Zonisamide Capsules

Healthy

United States
Mutual Pharmaceutical Company, Inc.

Completed

Fasting Bioavailability Study of Zonisamide Capsules

Healthy
Mutual Pharmaceutical Company, Inc.

Completed

Fed Bioavailability Study of Lovastatin Tablets and Mevacor Tablets

Healthy

Canada
Mutual Pharmaceutical Company, Inc.

Completed

Fasting Bioavailability Study of Lovastatin Tablets and Mevacor Tablets

Healthy

Canada
Mutual Pharmaceutical Company, Inc.

Completed

Fasted Bioequivalence Study of Primidone Tablets and Mysoline Tablets

Therapeutic Equivalency
Mutual Pharmaceutical Company, Inc.

Completed

Fasted Bioavailability Study of Cilostazol Tablets, 50mg

Therapeutic Equivalency, Healthy
Mutual Pharmaceutical Company, Inc.

Completed

Fasted Bioavailability Study of Cilostazol Tablets, 100 mg

Therapeutic Equivalency
Mutual Pharmaceutical Company, Inc.

Completed

Bioequivalence Study of Fenofibric Acid Versus Tricor® (Fenofibrate)

Healthy

United States
Mutual Pharmaceutical Company, Inc.

Completed

Fed Bioequivalence Study of Fenofibric Acid Versus TriCor® (Fenofibrate)

Healthy
Chonnam National University Hospital
Institute of Bioequivalence and Bridging Study, College of Pharmacy, CNU

Completed

Bioequivalence of Rebamipide in Korean

Pharmacogenetics | Therapeutic Equivalency

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

Completed

Study Comparing Two Manufacturing Processes for Levonorgestrel 90 mg/Ethinyl Estradiol 20 mg (LNG/EE) in Healthy, Cycling Women

Healthy

United States
University of Ottawa

Completed

Comparison of the Pharmacokinetics of Two Generic Antidepressants and Their Respective Brand Preparations

Healthy

Canada
University Hospital Freiburg
Novartis

Completed

Pharmacokinetics of Two Extended-Release Formulations of Methylphenidate in Children With Attention Deficit Hyperactivity Disorder (ADHD) (MPH-Kinetics)

Attention Deficit Hyperactivity Disorder

Germany

Search clinical trials for: Therapeutic Equivalency

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