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Clinical Trial Summary

This study will be conducted at multiple sites and every patient will get treated with PTG-300. The objective of the study is to assess the effect of PTG-300 in treating adult hereditary hemochromatosis patients.


Clinical Trial Description

This study is a multicenter, open-label study. The objective of the study is to assess the effect of PTG-300 on transferrin saturation (TSAT) and serum iron in adult hereditary hemochromatosis patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04202965
Study type Interventional
Source Protagonist Therapeutics, Inc.
Contact
Status Completed
Phase Phase 2
Start date March 19, 2020
Completion date February 15, 2022

See also
  Status Clinical Trial Phase
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Unknown status NCT01398644 - Erythrocytapheresis Versus Phlebotomy as Maintenance Therapy in Hereditary Hemochromatosis (HH) Patients Phase 3
Terminated NCT05238207 - A Study to Evaluate BBI-001 in Hereditary Haemochromatosis (HH) Patients and Iron Deficient Volunteers Phase 1
Enrolling by invitation NCT05742035 - Quality and Biologic Characteristics of Red Blood Concentrates Obtained From Individuals With Elevated Ferritin. N/A
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