Search clinical trials for: BIOEQUIVALENCE

Total 2065 results

Respirent Pharmaceuticals Co Ltd.
Becro Ltd.

Active, not recruiting

A Bioequivalence Study Between Fluticasone Propionate 250 mcg and Salmeterol Xinafoate 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUS® 250/50 Inhalation Powder/GSK in Healthy Volunteers

Asthma | Bioequivalence

Greece
Laboratorios Andromaco S.A.

Completed

Bioavailability of Duloxetine 60 mg With Regards to Reference Product in Feeding Conditions

Bioequivalence

Chile
Laboratorios Andromaco S.A.

Completed

Bioavailability of Duloxetine 60 mg With Regards to Reference Product in Fasting Conditions

Bioequivalence

Chile
Laboratorios Andromaco S.A.

Completed

Bioavailability of Clormadinone/Ethinyl Estradiol Tablets 2 mg/0.02 mg With Regards to Reference Product

Bioequivalence

Chile
Lupin, Inc.

Completed

Clinical Endpoint Bioequivalence Study of Test and Reference Inhalation Products in Patients With COPD With Device Robustness

Chronic Obstructive Pulmonary Disease

United States
Centre of Clinical Pharmacology, Hanoi Medical...

Completed

An in Vivo Bioequivalence Study of 2 Loxoprofen Sodium Products in Vietnamese Healthy Male Volunteers

Bioequivalence

Vietnam
SecuraBio

Completed

Bioequivalence of Duvelisib and Food Effect on Pharmacokinetics of IPI-145

Healthy

United States
Radboud University Medical Center

Completed

Bioequivalence of Crushed Stribild With a Normal Breakfast or With Drip Feed Compared to the Whole Tablet (CRUSTRI)

HIV

Netherlands
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study Comparing A New 10 Mg Atorvastatin Tablet To A 10 Mg Atorvastatin Commercial Tablet

Hypercholesterolemia

United States
Respirent Pharmaceuticals Co Ltd.
Becro Ltd.

Completed

Pooled Analysis FP_SX_250_50

Asthma

Greece
Respirent Pharmaceuticals Co Ltd.
Becro Ltd.

Completed

A Pilot Bioequivalence Study Between Fluticasone Propionate 500 mcg and Salmeterol Xinafoate 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUS® 500/50 Inhalation Powder/GSK in Healthy Volunteers

Bioequivalence

Greece
Respirent Pharmaceuticals Co Ltd.
Becro Ltd.

Completed

A Pivotal Bioequivalence Study Between Fluticasone Propionate 250 mcg and Salmeterol Xinafoate 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUS® 250/50 Inhalation Powder/GSK in Healthy Volunteers

Bioequivalence

Greece
Pfizer

Completed

A Study to Determine the Bioequivalence of Two Doses of Tafamidis

Healthy

United States
Akorn, Inc.

Completed

Bioequivalence Study With Clinical Endpoint for Diclofenac Sodium Topical Gel 1%

Osteoarthritis, Knee

Estonia, Poland, Latvia, Lithuania, Romania, Ukraine
Merck Healthcare KGaA, Darmstadt, Germany, an affiliate...

Completed

Deflox Tablets Bioequivalence (BE) Trial

Healthy

Mexico
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study Comparing A New 80 Mg Atorvastatin Tablet To A 80 Mg Atorvastatin Commercial Tablet

Hypercholesterolemia

United States
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study Of Pediatric Appropriate Formulation

Hypercholesterolemia

United States
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study On Pediatric Appropriate Formulation

Hypercholesterolemia

Singapore
Pharmtechnology LLC
ClinPharmInvest, LLC

Unknown

Bioequivalence Study of Two Formulations of Rivaroxaban Tablets 10 mg in Healthy Male Volunteers in Fasting Conditions

Bioequivalence

Russian Federation
Pfizer's Upjohn has merged with Mylan to form Viatris...

Withdrawn

A Bioequivalence Study of Sildenafil Citrate Orally-Disintegrating Film Dosage Form

Healthy
Laboratorios Andromaco S.A.

Completed

Bioavailability of Levonorgestrel/Ethinyl Estradiol Tablets 0.1 mg/0.02 mg With Regards to Reference Product

Bioequivalence

Chile
Shenzhen Salubris Pharmaceuticals Co., Ltd.

Completed

Bioequivalence Study of SAL001 and FORSTEO in Healthy Chinese Adults

Postmenopausal Osteoporosis

China
Pfizer

Completed

Study To Assess The Bioequivalence Under Fed And Fasted Conditions Of The Fesoterodine Beads-In-Capsule SR4 And SR7 Formulations And To Estimate The Bioavailability of SR7 Beads Sprinkled On Apple Sauce Relative To The Beads-In-Capsule SR7 Formulation Administer

Neurogenic Detrusor Overactivity

Belgium
Laboratorios Andromaco S.A.

Completed

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

Bioequivalence

Chile
Dong-A ST Co., Ltd.

Completed

Bioequivalence Study Between "DA-5209 Tab" and "Lixiana Tab"

Healthy

Korea, Republic of
LG Chem

Completed

Bioequivalence Study for Fixed Dose Combination Zemimet® SR Tab. 50/1000 and Coadministration of Gemigliptin 50 mg and Metformin 1000 mg.

Type 2 Diabetes

Thailand
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

A Pivotal Bioequivalence Study Between The Sildenafil Powder For Oral Suspension (10 Mg/Ml) And The Sildenafil 10 Mg Immediate Release (IR) Tablet Relative To The Revatio 20 Mg IR Tablet In Healthy Volunteers Under Fasting Conditions

Pulmonary Arterial Hypertention

Belgium
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study Of Gabapentin Between Tablet And Liquid Formulation And The Food Effect Study Of Liquid Formulation

Healthy

Singapore
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Pharmacokinetics Of Sildenafil Orally Disintegrating Tablet Formulation Versus To Viagra® Oral Tablet.

Erectile Dysfunction

Singapore
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study of Doxazosin 4 Mg Orally-Disintegrating Tablet With Or Without Water To Doxazosin 4 Mg Japanese Marketed Immediate Release Tablet Under Fasted Condition

Hypertension

Japan
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence of Alprazolam Sublingual vs Oral Tablets

Healthy

India
Pfizer's Upjohn has merged with Mylan to form Viatris...

Withdrawn

Bioequivalence Of A Test Alprazolam Sublingual Formulation Compared To A Commercial Sublingual Formulation

Healthy
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

A Bioequivalence Study Of A New Alprazolam Dropped Formulation Versus Alprazolam Tablets

Healthy

Brazil
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Pharmacokinetics Of Alprazolam Sublingual Tablet Versus Conventional Tablet

Anxiety Disorder

United States
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

A Study to Assess if Epanutin Infatabs 50 mg From Germany Are Similar to Dilantin Infatabs 50 mg From Australia

Healthy

Singapore
Pfizer's Upjohn has merged with Mylan to form Viatris...

Withdrawn

Bioequivalence of a New and a Commercial Alprazolam Sublingual Formulation

Healthy
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study For 5 Mg Amlodipine Orally-Disintegrating Tablet

Healthy

Japan
Pfizer's Upjohn has merged with Mylan to form Viatris...

Withdrawn

Bioequivalence of a New Sublingual and a Reference Alprazolam Immediate Release Tablet Formulation

Healthy
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

An Bioequivalence Study Of Xanax Extended Release Tablets From Two Different Manufacturing Sites

Healthy Subjects

Singapore
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study For Orally-Disintegrating Tablet Of Sildenafil

Healthy

Japan
Pfizer's Upjohn has merged with Mylan to form Viatris...
Investigacion Farmacologica y Biofarmaceutica, S.A. de C.V.

Withdrawn

A Study Of Two Oral Preparations Of 2 Mg Alprazolam In Healthy Volunteers Under Fasting Conditions

Healthy
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

An Bioequivalence Study Comparing Nicergoline 10 mg Tablet Manufactured in China With Nicergoline 10 mg Tablet Manufactured in Italy Under Fasted and Fed Conditions in Healthy Chinese Participants

Pharmacokinetics

China
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study Of PHENYTOIN Suspension Made By Pfizer, Versus EPAMIN® Made By McNeil LA LLC In Healthy Volunteers Under Fasting Conditions

Healthy

Mexico
Akorn, Inc.
South Florida Family Health and Research Centers; Axis Clinical Trials

Completed

Bioequivalence Study for Benzyl Alcohol Lotion 5%.

Head Lice

United States
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Study Of Phenytoin Suspension Versus Epamin® In 34 Healthy Volunteers.

Healthy

Mexico
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

A Study Comparing the Drug Exposure in Humans After Administration of a 50 mg Tablet of Sertraline Hydrochloride as Compared to a 50 mg Capsule of Sertraline Hydrochloride Under Fasted (Nonfed) Conditions

Healthy

Singapore
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Bioequivalence Of Zoloft ODT To Jzoloft In Healthy Japanese Subjects

Healthy

Japan
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

Investigation Of Absorption And Pharmacokinetics Of A Single Dose Of Controlled Release Pregabalin Tablet Administered Fasted In The Evening or Immediately Following A 600-750 Calorie Evening Meal As Compared To Single Dose Of Immediate Release Pregabalin Capsule In Healthy Volunteers

Healthy

United States
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

An Investigation of the Effects of Erythromycin on the Pharmacokinetics of the Pregabalin Controlled Release Tablet

Healthy

Belgium
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

An Investigation Of The Absorption And Pharmacokinetics Of Multiple Doses Of A Controlled Release Pregabalin Tablet As Compared To Multiple Doses Of The Immediate Release Pregabalin Capsule

Healthy

Belgium

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