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NCT07332091Possibly a fitRecruiting

Study of vamifeport for adults with iron overload from hereditary hemochromatosis

Homeostatic Iron Regulator Gene-related Hereditary Hemochromatosis

Part of Genetic & congenital, Hormones & metabolism clinical trials.

This study tests an investigational drug called vamifeport to see if it can reduce iron levels in the body and improve outcomes for people with hereditary hemochromatosis (a genetic condition causing too much iron absorption). Participation may help manage iron overload and potentially reduce the need for regular blood removal treatments.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
84 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be 18 years or older.
  • You must have a confirmed diagnosis of hereditary hemochromatosis (specifically the HFE type).
  • You must have iron overload, shown by blood tests (TSAT > 45% and ferritin between 200 and 5000 ng/mL) and an MRI of the liver showing iron levels in a specific range.
  • Your body mass index (BMI) must be between 18.5 and 34.9.
  • You must not have other significant medical conditions or abnormal test results that could affect your safety or the study results.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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