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Bioequivalence

Clinical trial condition

Bioequivalence

Explore clinical trials studying Bioequivalence. Study availability and eligibility vary by location and protocol.

143 public trials 2 recruiting studies

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Bioequivalence trial results

Completed

The Bioequivalence Study of Two Different Formulations of Candesartan Cilexetil After a Single Oral Dose Administration Under Fasting Conditions

NCT04012307

Conditions: Bioequivalence
Locations: Altasciences Company Inc. Mount Royal, Quebec, Canada

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Completed

Bioequivalence Study of Bosentan 125 mg Tablets Immediate Release (IR) Versus Tracleer® 125 mg Tablets IR In Healthy Subjects

NCT04101370

Conditions: Behavior, Bioequivalence, Fasting, +1 more
Locations: Clinical Hospital № 3 Yaroslavl, Russia

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Completed

Rivastigmine Bioequivalence Trial With Multiple Application of Transdermal Patches (9.5mg/24h)

NCT03659435

Conditions: Bioequivalence
Locations: SocraTec R&D GmbH, Clinical Pharmacology Unit Erfurt, Thuringia, Germany

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Completed

A Bioequivalence Study Between Fluticasone Propionate 100 mcg and Salmeterol Xinafoate 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUS® 100/50 Inhalation Powder/GSK in Healthy Volunteers

NCT03975166

Conditions: Bioequivalence
Locations: BECRO Clinical Facility Larissa, Thessaly, Greece

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Completed

The Bioequivalence Study of Two Different Formulations of Olmesartan Medoxomil After a Single Oral Dose Administration Under Fasting Conditions.

NCT03951051

Conditions: Bioequivalence
Locations: Altasciences Company Inc. Mount Royal, Quebec, Canada

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Completed

Bioequivalence Study of Two Formulations of Febuxostat 120 mg Film-coated Tablets in Healthy Adult Volunteers After a Single Oral Dose Administration Under Fasting Conditions

NCT03918551

Conditions: Bioequivalence
Locations: Altasciences Company Inc. Montreal, Quebec, Canada

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Completed

Pharmacokinetic and Pharmacodynamic Assessment of a Novel, Pharmaceutical Lipid-Aspirin Complex

NCT04008979

Conditions: Bioequivalence
Locations: Not specified

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Completed

Bioequivalence Study of Sotalol, Tablets, 160 mg (Pharmtechnology LLC, Belarus), and Sotalex ®, Tablets, 160 mg (Bristol-Myers Squibb GmbH & Co. KGaA, Germany), in Healthy Volunteers Under Fasting Conditions

NCT03799536

Conditions: Bioequivalence
Locations: National Anti-Doping Laboratory Settl.Lesnoy, Minsk Oblast, Belarus

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Completed

Bioequivalence Study of Two Formulations of Propafenone 300 mg Film-coated Tablets in Healthy Adult Volunteers After a Single Oral Dose Administration Under Fasting Conditions

NCT03915340

Conditions: Bioequivalence
Locations: Altasciences Company Inc. Mount Royal, Quebec, Canada

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Completed

A Bioequivalence Study Between Fluticasone Salmeterol Xinafoate vs. SERETIDE DISKUS® in Healthy Volunteers With Charcoal Blockade (BREATH-PK250-CC)

NCT03894280

Conditions: Bioequivalence
Locations: BECRO Clinical Facility Larissa, Thessaly, Greece

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