Found 18 matching trials
A Study to Assess the Efficacy and Safety of a Subcutaneous Formulation of Efgartigimod PH20 SC in Adults With Pemphigus (Vulgaris or Foliaceus) PHASE3 This is a prospective, multicenter, randomized, double-blinded, placebo-con...
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Investigator site 77 - US0010086
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A Study to Investigate the Efficacy and Safety of Efgartigimod PH20 SC in Adult Participants With Active Idiopathic Inflammatory Myopathy. PHASE2 This study's purpose is to measure the treatment response from efgartigimod...
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Neuromuscular Research Center
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Study of the Intradermal Injection of rHuPH20 or Placebo in Participants With Nickel Allergic Contact Dermatitis PHASE2 The purpose of this study is to compare the effect and safety of rHuPH20 or...
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Symbio Phase I Unit, Saint Anthony Memorial Research Center
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A Study of PEGylated Recombinant Human Hyaluronidase in Combination With Nab-Paclitaxel Plus Gemcitabine Compared With Placebo Plus Nab-Paclitaxel and Gemcitabine in Participants With Hyaluronan-High Stage IV Previously Untreated Pancreatic Ductal Adenocarcinoma PHASE3 The purpose of this study is to compare the efficacy and safety of PEGylate...
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University of South Alabama
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A Phase 2/3 Study of Efgartigimod PH20 SC in Adult Participants With Bullous Pemphigoid PHASE2 ARGX-113-2009 is an operationally seamless 2-part, phase 2/3, prospective, ...
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Investigator site 74 - US0010178
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First Time in Human Study of Long Acting VH4524184 Formulations PHASE1 The purpose of this study is to identify 1 or more doses of parenterally ad...
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GSK Investigational Site
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Study of Gemcitabine + PEGPH20 vs Gemcitabine Alone in Stage IV Previously Untreated Pancreatic Cancer PHASE1 Phase 1B: Open label (all patients receive PEGPH20+gemcitabine), dose escal...
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Highlands Oncology Group
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Pharmacokinetic and Safety Study of HYLENEX Recombinant-Augmented Subcutaneous Ceftriaxone Administration PHASE1 The objectives of this study are:
* to establish the safety of subcutaneou...
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Multiple Locations
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SAD and MAD Study With IV and SC Doses of ARGX-117 PHASE1 This is a phase 1, first-in-human, double-blinded, randomized, placebo-cont...
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Investigator Site 1
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Study to Evaluate Pharmacokinetic (PK), Safety and Tolerability of Cabotegravir (CAB) 400 Milligrams Per Milliliter (mg/mL) Formulation in Healthy Adult Participants PHASE1 This is an active control, randomized study to investigate the safety, tole...
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GSK Investigational Site
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