Last updated on July 2019

A Study to Assess the Efficacy Safety and Tolerability of KPL-716 in Reducing Pruritus in Prurigo Nodularis


Brief description of study

Study of the efficacy, safety, tolerability, pharmacokinetics (PK) and immunogenicity of KPL-716 in subjects with prurigo nodularis.

Detailed Study Description

This is a Phase 2a/b randomized, double-blind, placebo-controlled study to investigate the efficacy, safety, tolerability, PK and immunogenicity of KPL-716 administered subcutaneously (SC) in subjects with prurigo nodularis experiencing pruritus. The Phase 2a portion of the study will enroll up to 100 subjects and will include 2 arms: one active arm and one placebo arm.

Following analysis of the Phase 2a portion of the study (milestone dates above), enrollment into the Phase 2b portion may be initiated.

Clinical Study Identifier: NCT03816891

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Study Site 104

Anniston, AL United States
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Site 125

Phoenix, AZ United States
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Site 127

Scottsdale, AZ United States
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Site 116

Fountain Valley, CA United States
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Study Site 102

Los Angeles, CA United States
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Study Site 107

Largo, FL United States
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Site 111

Pembroke Pines, FL United States
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Site 117

Tampa, FL United States
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Site 105

Boise, ID United States
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Site 110

Beverly, MA United States
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Site 113

Fort Gratiot, MI United States
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Site 118

Troy, MI United States
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Site 108

Omaha, NE United States
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Site 121

Fairborn, OH United States
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Study Site 101

Houston, TX United States
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Site 106

Pflugerville, TX United States
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Site 128

San Antonio, TX United States
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Site 115

Spokane, WA United States
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Site 301

Red Deer, AB Canada
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Site 306

Fredericton, NB Canada
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Site 305

London, ON Canada
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Site 131

West Palm Beach, FL United States
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Site 114

Sandy Springs, GA United States
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Site 123

New Albany, IN United States
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Site 130

Warren, MI United States
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Site 302

Edmonton, AB Canada
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Site 307

Barrie, ON Canada
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Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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