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Clinical Trial Summary

According to the Respreeza® Summary of Product Characteristics, the initial infusions must be administered under the supervision of a health professional experienced in the treatment of alpha-1 antitrypsin deficiency, although subsequent infusions may be administered at home by the person responsible for care or by the patient. Clinical data on self-administration of Respreeza® are however limited and the grounds for self-administration are left to the assessment of the attending physician, who needs to ensure that appropriate training is delivered. In this context, CSL Behring would like to run a clinical study in order to assess the effectiveness of a home self-administration learning program in terms of switching to self-administration, and the long term maintenance of this administration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04262284
Study type Observational
Source CSL Behring
Contact
Status Active, not recruiting
Phase
Start date October 18, 2019
Completion date March 31, 2025

See also
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