Condition: Acute Intermittent Porphyria (AIP) · Sponsor: Icahn School of Medicine at Mount Sinai
This study proposes to identify the predisposing/protective modifying genes that underlie the acute attacks in symptomatic patients with Acute Intermittent Porphyria (AIP), an autosomal dominant inborn error of heme biosynthesis.
This description comes directly from the study's public registry record.
Chloe Cheung · 646-369-2045 · chloeyihang.cheung@mssm.edu
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| Icahn School of Medicine at Mount Sinai | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05502133