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Clinical trial

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 (Subcutaneous Immunoglobulin, Hizentra®) in Adults With Dermatomyositis (DM) - The RECLAIIM Study

NCT04044690 is registered in ClinicalTrials.gov with CSL Behring as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 (Subcutaneous Immunoglobulin, Hizentra®) in Adults With Dermatomyositis (DM) - The RECLAIIM Study
Lead sponsor
CSL Behring
Phase
Phase 3
Overall status
Terminated
Start date
October 21, 2019
Completion date
December 2, 2024
Enrollment
134 (actual)
Sites
76

Conditions

As the registry lists them; a condition with its own page is linked.