Condition: Homozygous Familial Hypercholesterolemia · Sponsor: Arrowhead Pharmaceuticals
This multicenter, randomized, placebo-controlled study will evaluate the efficacy and safety of zodasiran subcutaneous (SC) injection in subjects 12 years of age and older with genetically or clinically diagnosed Homozygous familial hypercholesterolemia (HoFH). After completion of the double blind (DB) treatment period subjects will be eligible to continue in the optional open-label extension (OLE) period of the study. All placebo subjects who opt to continue will transition to active drug during the OLE Period.
This description comes directly from the study's public registry record.
Medical Monitor · 626-304-3400 · YOSEMITE@arrowheadpharma.com
Always discuss trial participation with your own doctor first.
| Research Site 7 | Park Ridge, Illinois, United States | Recruiting |
| Research Site 2 | New York, New York, United States | Recruiting |
| Research Site 1 | Cincinnati, Ohio, United States | Recruiting |
| Research Site 14 | Pittsburgh, Pennsylvania, United States | Recruiting |
| Research Site 13 | Camperdown, New South Wales, Australia | Recruiting |
| Research Site 9 | Saint Leonards, New South Wales, Australia | Recruiting |
| Research Site 21 | Heidelberg, Victoria, Australia | Recruiting |
| Research Site 3 | Nedlands, Western Australia, Australia | Recruiting |
| Research Site 40 | Innsbruck, Austria | Recruiting |
| Research Site 39 | Linz, Austria | Recruiting |
| Research Site 42 | Vienna, Austria | Recruiting |
| Research Site 37 | Vienna, Austria | Recruiting |
+ 31 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07037771