drugset / Trial / NCT03686969
Study Evaluating Efficacy and Safety of Octanorm in Patients With Dermatomyositis
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Octanorm | Protein / enzyme biologic | 0.5 g/kg | Subcutaneous |