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Atransferrinemia
MONDO:0008846Congenital atransferrinemia is a very rare hematologic disease caused by a transferrin (TF) deficiency and characterized by microcytic, hypochromic anemia (manifesting with pallor, fatigue and growth retardation) and iron overload, and that can be fatal if left untreated.
Also known as: atransferrinemia, congenital atransferrinemia, congenital hypotransferrinemia, familial hypotransferrinemia, hereditary atransferrinemia, hypotransferrinemia, familial, transferrin serum level quantitative trait locus 1
10 clinical trials for this condition and its sub-types, 1 tagged with Atransferrinemia itself.
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Missing Iron-Carrying protein replaced in rare blood disorder
Cure OngoingAtransferrinemia is a rare inherited condition in which the body cannot make enough transferrin, a protein that moves iron through the blood. Without it, iron builds up in organs and red blood cells cannot form properly. Researchers are testing intravenous infusions of apotransfe…
Phase 2 • Sponsor: Prothya Biosolutions • Aim: Cure
Last updated Sep 18, 2026 00:00 UTC
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New blood treatment could block zika in transfusions
Disease control OngoingThis study tests a special treatment for red blood cells that aims to kill the Zika virus, making transfusions safer. About 692 people who need blood transfusions will receive either treated or standard blood. The goal is to see if the treated blood works just as well and is safe…
Phase 3 • Sponsor: Cerus Corporation • Aim: Disease control
Last updated Jun 27, 2026 11:03 UTC