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Clinical Trial Summary

This study is a Phase 2 multicenter, randomized, placebo controlled, single-blind study. The primary objective of the study is to compare the effect of weekly dosing of LJPC-401 (synthetic human hepcidin) versus placebo on transferrin saturation (TSAT) in an adult hereditary hemochromatosis patient population.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03395704
Study type Interventional
Source La Jolla Pharmaceutical Company
Contact
Status Completed
Phase Phase 2
Start date November 29, 2017
Completion date October 28, 2019

See also
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Completed NCT03203850 - Study to Evaluate the Efficacy and Safety of Deferasirox Film-coated Tablet Versus Phlebotomy in Patients With Hereditary Hemochromatosis (HH) Phase 2
Completed NCT00068159 - Cardiac Function in Patients With Hereditary Hemochromatosis
Completed NCT00395629 - Safety and Efficacy of Deferasirox (ICL670) in Patients With Iron Overload Resulting From Hereditary Hemochromatosis Phase 1/Phase 2
Completed NCT00440986 - Clinical Management of Hereditary Hemochromatosis: Phlebotomy vs. Erythrocytoapheresis Phase 2/Phase 3