Condition: Alpha1-Antitrypsin Deficiency · Sponsor: Grifols Therapeutics LLC
The purpose of this study is to evaluate the safety and tolerability of 72 milligrams per kilogram (mg/kg) and 180 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).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
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| UCLA Medical Center | Los Angeles, California, United States | — |
| University of Florida | Gainesville, Florida, United States | — |
| University of Miami | Miami, Florida, United States | — |
| Cleveland Clinic | Cleveland, Ohio, United States | — |
| Medical University of South Carolina - Children's Hospital | Charleston, South Carolina, United States | — |
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Source record: clinicaltrials.gov/study/NCT04722887