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Spots Global Cancer Trial Database for Intravenous Iloprost in Subjects With Symptomatic Raynaud's Phenomenon Secondary to Systemic Sclerosis (Phase 2)

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Intravenous Iloprost in Subjects With Symptomatic Raynaud's Phenomenon Secondary to Systemic Sclerosis (Phase 2)

Official Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Phase 2 Pilot Study Evaluating Intravenous Iloprost in Subjects With Symptomatic Raynaud's Phenomenon Secondary to Systemic Sclerosis

Study ID: NCT03867097

Study Description

Brief Summary: This is a Phase 2, multicenter, double-blind, randomized, placebo-controlled study to evaluate the effect of iloprost on the symptomatic relief of Raynaud's Phenomenon attacks in subjects with symptomatic Raynaud's Phenomenon secondary to Systemic Sclerosis.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arizona Arthritis & Rheumatology Research, PLLC, Phoenix, Arizona, United States

Pacific Arthritis Care Center of Los Angeles, Los Angeles, California, United States

Stanford University Medical Center, Palo Alto, California, United States

University of California San Francisco, San Francisco, California, United States

Georgetown University Medical Center - Department of Rheumatology, Washington, District of Columbia, United States

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

University of Michigan, Ann Arbor, Michigan, United States

Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States

Hospital for Special Surgery, New York, New York, United States

Columbia University Medical Center, New York, New York, United States

Cleveland Clinic, Cleveland, Ohio, United States

The University of Toledo Medical Center (UTMC) - Ruppert Health Center, Toledo, Ohio, United States

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

University of Texas Houston - Division of Rheumatology and Clinical Immunogenetics, Houston, Texas, United States

Virginia Mason Medical Center, Seattle, Washington, United States

Arthritis Northwest Rheumatology PLLC, Spokane, Washington, United States

Contact Details

Name: Wade Benton, Pharm D

Affiliation: Civibio Pharma, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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