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- US Clinical Trials Registry
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Clinical Trials on Bioequivalence in United States
Total 38 results
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Indiana UniversityFood and Drug Administration (FDA)Completed
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KBP BiosciencesMedpace, Inc.Completed
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Repros Therapeutics Inc.Completed
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Janssen Research & Development, LLCCompleted
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University of FloridaFood and Drug Administration (FDA)CompletedBioequivalenceUnited States
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University of Maryland, BaltimoreFood and Drug Administration (FDA)Completed
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PLx PharmaCompletedBioequivalenceUnited States
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argenxCompleted
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AstraZenecaCompletedBioequivalenceUnited States
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Coherus Biosciences, Inc.Completed
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Teva Pharmaceuticals USACompletedBioequivalenceUnited States
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Zogenix, Inc.CompletedPharmacokinetics | BioequivalenceUnited States
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Taro Pharmaceuticals USAWAYCroCompletedBioequivalence StudyUnited States
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Baxter Healthcare CorporationQuotient SciencesCompletedBioequivalanceUnited States
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WockhardtWithdrawnBioequivalence in Healthy SubjectsUnited States
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H. Lundbeck A/SWithdrawn
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AstraZenecaCompletedBioequivalence, AUC, Cmax, PharmacokineticsUnited States
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WockhardtWithdrawnBioequivalence in Healthy SubjectsUnited States
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WockhardtWithdrawnBioequivalence in Healthy SubjectsUnited States
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Gedeon Richter Plc.CompletedBioequivalenceUnited Kingdom
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Cycle Pharmaceuticals Ltd.FARMOVS Clinical Research OrganisationCompletedBioequivalenceSouth Africa
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AstraZenecaCompletedHealthy Volunteers | BioequivalenceUnited Kingdom
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Church & Dwight Company, Inc.Medical University of South CarolinaCompletedBioequivalence of Vitamin D in Healthy AdultsUnited States
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Par Pharmaceutical, Inc.BASi Clinical Research UnitCompletedTo Determine Bioequivalence Under Fasting ConditionsUnited States
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NuPathe Inc.CompletedCompare Bioequivalence Patches Previously Used in the NP101-007 StudyUnited States
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Inflamax Research IncorporatedCompletedBioequivalence - Irritation and Sensitization Potential of Transdermal PatchUnited States, Canada
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Par Pharmaceutical, Inc.Cetero Research, San AntonioCompletedTo Determine the Bioequivalence Under Fasting ConditionsUnited States
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AstraZenecaCompletedPharmacokinetics | Bioequivalence | Healthy Japanese SubjectsUnited Kingdom
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AstraZenecaCompletedHealthy Volunteers Bioequivalence or Bioavailability StudyUnited Kingdom
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Taro Pharmaceuticals USACompleted
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Austarpharma, LLCUnknownBioequivalenceUnited States
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AstraZenecaCompletedBioequivalence, Log-transformed AUCss and Cmax,ss Values for Saxagliptin and MetforminUnited States
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Par Pharmaceutical, Inc.PharmaKinetics Laboratories Inc.CompletedTo Determine Bioequivalence Under Fed ConditionsUnited States
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Cycle Pharmaceuticals Ltd.FARMOVS Clinical Research OrganisationCompletedBioequivalenceSouth Africa
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AstraZenecaCompletedBioequivalence | Fixed Dose Combination Tablets | Healthy Male and Female SubjectsUnited States
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Biomedical Advanced Research and Development AuthorityRho Federal Systems Division, Inc.; AllucentNot yet recruitingAtropine BioequivalenceUnited States
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Xcovery Holdings, Inc.CompletedBioequivalencyUnited States