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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT03867097

Public ClinicalTrials.gov record NCT03867097. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 4:51 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03867097
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Civi Biopharma, Inc.
Industry
Enrollment
34 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 7, 2019 (Actual)
Primary completion
Aug 6, 2019 (Actual)
Completion
Aug 6, 2019 (Actual)
Last update posted
May 25, 2025

2019

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Arizona Arthritis & Rheumatology Research, PLLC Phoenix Arizona 85032 —
Pacific Arthritis Care Center of Los Angeles Los Angeles California 90045 —
Stanford University Medical Center Palo Alto California 94305 —
University of California San Francisco San Francisco California 94143 —
Georgetown University Medical Center - Department of Rheumatology Washington D.C. District of Columbia 20007 —
Johns Hopkins University School of Medicine Baltimore Maryland 21224 —
University of Michigan Ann Arbor Michigan 48109-5422 —
Robert Wood Johnson Medical School New Brunswick New Jersey 08903 —
Hospital for Special Surgery New York New York 10021 —
Columbia University Medical Center New York New York 10032 —
Cleveland Clinic Cleveland Ohio 44195 —
The University of Toledo Medical Center (UTMC) - Ruppert Health Center Toledo Ohio 43614 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15261 —
University of Texas Houston - Division of Rheumatology and Clinical Immunogenetics Houston Texas 77030 —
Virginia Mason Medical Center Seattle Washington 98101 —
Arthritis Northwest Rheumatology PLLC Spokane Washington 99204 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03867097, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 25, 2025 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03867097 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →