Found 27 matching trials
Study to Access the Relative Bioavailability of Subcutaneous Dose of Nemolizumab When Administered Via Auto-Injector Versus Dual-Chamber Syringe PHASE1 This study was to compare the rate and extent of absorption of a single dos...
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Galderma Investigational Site 7024
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To Assess the Patients' Ability to Self-Administer Fasinumab PHASE1 The primary objective is to demonstrate that the auto-injector(AI) is suita...
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Regeneron Research Facility
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A Study to Evaluate the Bioavailability of Risankizumab in Pre-filled Syringe or Auto-injector in Healthy Adult Participants PHASE1 The objective of this study is to evaluate the bioavailability of risankizu...
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Acpru /Id# 210844
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A Study to Compare the Auto-injector and Pre-filled Syringe of CT-P43 in Healthy Male Subjects PHASE1 This is phase 1 study to Compare the Pharmacokinetics, Safety and Immunogen...
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Korea University Guro Hospital
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A Study to Evaluate Usability of Subcutaneous Auto-injector of CT-P47 in Patients With Active Rheumatoid Arthritis PHASE3 This is a phase 3 study to evaluate the usability of the CT-P47 auto-inject...
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Multiple Locations
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A Study of Two Formulations of LY3074828 in Healthy Participants PHASE1 The purpose of this study is to look at the amount of the study drug, LY307...
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Covance Clinical Research Inc
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A Study to Evaluate the Safe and Effective Use of a Zilucoplan Auto-injector by Study Participants With Generalized Myasthenia Gravis PHASE3 The purpose of this study is to evaluate the effectiveness, safety and tole...
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A Study to Compare the Blood Level of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-injector in Adult Healthy Volunteer Participants PHASE1 The purpose of the study is to evaluate the pharmakokinetics (PK), safety, ...
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A Study to Compare the Auto-injector and Pre-filled Syringe of CT-P52 in Healthy Male Subjects PHASE1 This is phase 1 study to Compare the Pharmacokinetics, Safety and Immunogen...
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Korea University Guro Hospital
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A 12 Week Randomized Open Label Parallel Group Multicenter Study to Evaluate Bioequivalence of 20 mg Subcutaneous Ofatumumab Injected by Pre-filled Syringe or Autoinjector in Adult RMS Patients PHASE2 The primary purpose of this study is to demonstrate pharmacokinetic bioequi...
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Novartis Investigative Site
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