A Study to Evaluate Safety, Tolerability and Pharmacokinetics of Two Different Doses of Alpha1-Proteinase Inhibitor Subcutaneous (Human) 15% in Participants With Alpha1-Antitrypsin Deficiency

  • STATUS
    Recruiting
  • participants needed
    16
  • sponsor
    Grifols Therapeutics LLC
Updated on 30 March 2023

Summary

The purpose of this study is to evaluate the safety and tolerability of 72 milligrams per kilogram (mg/kg) and 144 mg/kg Alpha-1 15%, administered as a single-dose subcutaneous (SC) infusion and subsequently as weekly SC infusions over 8 weeks in participants with Alpha1-Antitrypsin Deficiency (AATD).

Details
Condition Alpha1-Antitrypsin Deficiency
Treatment Liquid Alpha1-Proteinase Inhibitor (Human), Alpha-1 15%
Clinical Study IdentifierNCT04722887
SponsorGrifols Therapeutics LLC
Last Modified on30 March 2023

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