A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Phase 3 Study Evaluating the Safety and Efficacy of Intravenous Iloprost in Subjects With Systemic Sclerosis Experiencing Symptomatic Digital Ischemic Episodes (AURORA Study)

Who is this study for? Adult patients with systemic sclerosis
What treatments are being studied? Iloprost
Status: Completed
Location: See all (30) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This is a Phase 3, multicenter, double-blind, randomized, placebo-controlled study to evaluate the safety and efficacy of iloprost on the frequency of and relief from symptomatic digital ischemic episodes in subjects with systemic sclerosis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• Male or female subjects must be greater than or equal to 18 years of age.

• Subjects must have a diagnosis of Systemic Sclerosis as defined by the 2013 American College of Rheumatology criteria/EULAR criteria

• Subjects must have a diagnosis or history of Raynaud's Phenomenon, self-reported or reported by a physician, with at least a 2-phase color change in finger(s) of pallor, cyanosis, and/or reactive hyperemia in response to cold exposure or emotion

• Subjects must have a minimum of 10 symptomatic Raynaud's Phenomenon attacks, documented in the electronic patient-reported outcomes (ePRO) diary, occurring over at least 3 separate days of the 3- to 5-day eligibility period

• Subjects must complete a minimum of 80% of the daily ePRO diary entry during the baseline period

• Female subjects of childbearing potential and male subjects must agree to use contraception for the duration of the study.

• Subjects must be willing and able to comply with the study requirements and give informed consent for participation in the study

Locations
United States
Arizona
Arizona Arthritis & Rheumatology Research, PLLC
Phoenix
Mayo Clinic - Scottsdale
Scottsdale
University of Arizona - Arthritis Research Center
Tucson
California
Cedars-Sinai Medical Center
Los Angeles
University of California, Los Angeles Medical Center
Los Angeles
Stanford University Medical Center
Palo Alto
University of California San Francisco
San Francisco
Washington, D.c.
Georgetown University Medical Center - Department of Rheumatology
Washington
Illinois
Northwestern Medical Faculty Foundation
Chicago
Louisiana
University Medical Center New Orleans
New Orleans
Massachusetts
Tufts Medical Center
Boston
Maryland
Johns Hopkins University School of Medicine
Baltimore
Michigan
University of Michigan
Ann Arbor
West Michigan Rheumatology PLLC
Grand Rapids
Minnesota
University of Minnesota Maple Grove
Minneapolis
Nebraska
University of Nebraska Medical Center
Omaha
New Jersey
Robert Wood Johnson Medical School
New Brunswick
New York
Columbia University Medical Center
New York
Hospital for Special Surgery
New York
Ohio
University of Cincinnati - Scleroderma Center
Cincinnati
Cleveland Clinic
Cleveland
Ohio State University
Columbus
The University of Toledo Medical Center (UTMC) - Ruppert Health Center
Toledo
Pennsylvania
University of Pennsylvania
Philadelphia
University of Pittsburgh Medical Center
Pittsburgh
South Carolina
Medical University of South Carolina (MUSC)
Charleston
Texas
University of Texas Houston - Division of Rheumatology and Clinical Immunogenetics
Houston
Utah
University of Utah
Salt Lake City
Washington
Virginia Mason Medical Center
Seattle
Wisconsin
Froedtert Hospital and the Medical College of Wisconsin
Milwaukee
Time Frame
Start Date: 2019-10-14
Completion Date: 2021-06-09
Participants
Target number of participants: 198
Treatments
Placebo_comparator: Placebo
Subjects will receive study drug for 5 consecutive days as an IV infusion over 6 hours each day via a peripheral line. Study drug will be initiated at a starting dose 0.5 ng/kg/min up to 2.0 ng/kg/min.
Active_comparator: Iloprost Injection, for intravenous use
Subjects will receive study drug for 5 consecutive days as an IV infusion over 6 hours each day via a peripheral line. Study drug will be initiated at a starting dose 0.5 ng/kg/min up to 2.0 ng/kg/min.
Sponsors
Leads: Eicos Sciences, Inc.

This content was sourced from clinicaltrials.gov

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