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Completed Phase 3 Interventional Results available

Study Evaluating Efficacy and Safety of Octagam 10% in Patients With Dermatomyositis (Idiopathic Inflammatory Myopathy)

ClinicalTrials.gov ID: NCT02728752

Public ClinicalTrials.gov record NCT02728752. 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 21, 2026, 9:47 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

Prospective, Double-blind, Randomized, Placebo-Controlled Phase III Study Evaluating Efficacy and Safety of Octagam 10% in Patients With Dermatomyositis ("ProDERM Study")

Brief summary

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

Prospective, Double-blind, Randomized, Placebo-Controlled Phase III Study Evaluating Efficacy and Safety of Octagam 10% in Patients With Dermatomyositis ("ProDERM study")

Study identification

NCT ID
NCT02728752
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Octapharma
Industry
Enrollment
95 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 79 Years
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
Feb 27, 2017 (Actual)
Primary completion
Nov 5, 2019 (Actual)
Completion
Nov 5, 2019 (Actual)
Last update posted
Dec 23, 2021

2017 – 2019

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
17
Facility City State ZIP Site status
Octapharma Research Site Huntington Beach California 92647 —
Octapharma Research Site Los Angeles California 90095 —
University of California -Irvine Orange California 92868 —
Octapharma Research Site Orlando Florida 32819 —
NeuroMedical Research Center Panama City Florida 32405 —
Octapharma Research Site Plantation Florida 33324 —
University of South Florida Tampa Florida 33612 —
Octapharma Research Site Kansas City Kansas 66160 —
Octapharma Research Site Ann Arbor Michigan 48109 —
Octapharma Research Site Rochester Minnesota 55905 —
Octapharma Research Site Great Neck New York 11021 —
Octapharma Research Site Portland Oregon 97239 —
Octapharma Research Site Pittsburgh Pennsylvania 15213 —
Stones River Dermatology Murfreesboro Tennessee 37130 —
Austin Neuromuscular Center Austin Texas 78756 —
Octapharma Research Site Houston Texas 77034 —
Arthritis & Osteoporosis Clinic Waco Texas 76710 —

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02728752, 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 Dec 23, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02728752 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →