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Withdrawn Phase 2 Interventional

Efficacy and Safety of IgPro10 in Adults With Systemic Sclerosis (SSc)

ClinicalTrials.gov ID: NCT04138485

Public ClinicalTrials.gov record NCT04138485. 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 Jul 22, 2026, 10:08 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 Randomized, Multicenter, Double-Blind, Placebo Controlled, Phase 2 Study to Evaluate the Efficacy and Safety of IgPro10 (Intravenous Immunoglobulin, Privigen®) for the Treatment of Adults With Systemic Sclerosis

Study identification

NCT ID
NCT04138485
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 2
Lead sponsor
CSL Behring
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • IgPro10 Biological
  • Placebo Biological

Biological

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
Dec 19, 2019
Primary completion
Sep 15, 2020
Completion
Sep 15, 2020
Last update posted
Nov 16, 2020

2019 – 2020

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
Mayo Clinic Arizona - Scottsdale Scottsdale Arizona 85259
Pacific Arthritis Care Center Los Angeles California 90045
University of California Los Angeles California 90095
Stanford University Medical Center Palo Alto California 94304
University of Colorado Aurora Colorado 80045
Lombardi Cancer Center-Georgetown University Washington D.C. District of Columbia 20007
Alliance for Multispecialty Research Wichita Kansas 67207
Heartland Research Associates, LLC Wichita Kansas 67207
Louisiana State University Health Sciences Center Shreveport Louisiana 71103
John Hopkins Bayview Medical Center Baltimore Maryland 21287
Boston University Amyloidosis Center Boston Massachusetts 02118
University of Michigan Health System Ann Arbor Michigan 48108
Rutgers Clinical Research Center New Brunswick New Jersey 08901
Northwell Health Great Neck New York 11021
Hospital For Special Surgery New York New York 10021
Cleveland Clinic - Taussig Cancer Center Cleveland Ohio 44195
Altoona Center For Research Duncansville Pennsylvania 16635
University of Pennsylvania - Perelman Center Philadelphia Pennsylvania 19104
Medical University of South Carolina Charleston South Carolina 29425
The University Of Texas Medical School At Houston (Utms) Houston Texas 77030

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 57 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04138485, 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 Nov 16, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04138485 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →