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Bioequivalence Study in Healthy Subjects
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Bioequivalence Study in Healthy Subjects trials you may qualify forClinical trial pipeline · Data from ClinicalTrials.gov
See which Bioequivalence Study in Healthy Subjects trials you may qualify forThe purpose of this research study is to compare the bioavailability and adhesion of a generic Selegiline transdermal system (TDS) against the marketed comparat…
This two-part study will evaluate the bioequivalence, safety, and tolerability of a single SC dose of trastuzumab administered via handheld syringe/syringe pump…
In this study, researchers will learn more about BIIB141, also known as omaveloxolone or SKYCLARYS®. This drug has been approved, or made available for doctors…
The main purpose of this study is to assess the safety and tolerability of mirikizumab (LY3074828) solution formulation administered as a single injection compa…
This study will investigate the bioequivalence between two formulations of HRS-1893 tablets. Safety and tolerability will also be assessed.
The goal of this study is to learn what happens to MK-7240 in a healthy person's body over time (pharmacokinetic or PK study). Researchers also want to learn ab…
The purpose of this study is to assess the bioequivalence (medicines that may have different names or be made in different ways, but have the same effect on the…
This study evaluated the bioequivalence and safety of the test formulation (Tenofovir Disoproxil Fumarate Tablets, Haisco Pharmaceutical Group Co., Ltd.) and th…