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A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 in Adults With Dermatomyositis (DM)

Terminated · Phase 3 · NCT04044690

Conditions: Dermatomyositis

At a glance

Research payments reported, 2025
$239,589
U.S. investigators named
14
Sites paid
14
Planned or actual enrollment
134

About the trial

Sponsor
CSL Behring
Tested
human immunoglobulin G (drug), Placebo (drug)
Dates
Started 2019-10-21; completion 2024-12-02
Results posted
Yes

This is a phase 3, multicenter, randomized, placebo-controlled, double-blind study of IgPro20 (subcutaneous Ig) treatment in adult subjects with dermatomyositis (DM). The primary objective of this study is to assess the efficacy of IgPro20 subcutaneous (SC) doses in comparison to placebo in adult subjects with DM, as measured by responder status based on Total Improvement Score (TIS) assessments.

From ClinicalTrials.gov, last updated 2025-12-09. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Csl Behring reported $239,589 in research payments for this study in 2025 (102 payments).

Products named: Hizentra

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.