drugset / Trial / NCT03686969

Study Evaluating Efficacy and Safety of Octanorm in Patients With Dermatomyositis

NCT03686969 ↗

Phase 3 Terminated 1 enrolled Octapharma
RandomizedParallel-groupDouble-blindTreatment

Summary

DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED PHASE III STUDY EVALUATING EFFICACY AND SAFETY OF SUBCUTANEOUS HUMAN IMMUNOGLOBULIN (OCTANORM) IN PATIENTS WITH DERMATOMYOSITIS

Timeline

Start
2018-08-02
Primary completion
2018-11-22
Completion
2018-11-29

Outcome

Outcome not reported

Stopped (Enrollment): “Study complexity, low study recruitment”

Drugs

EvaluationDrugModalityDoseRoute
Subject Octanorm Protein / enzyme biologic 0.5 g/kg Subcutaneous

Indications