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.
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 Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
16
Active treatment with PTG-300 injected subcutaneously.
Protagonist Investigational Site
Fayetteville, Georgia, United States
Protagonist Investigational Site
Bethesda, Maryland, United States
Protagonist Investigational Site
Charlotte, North Carolina, United States
Effect of PTG-300 on Transferrin Saturation
Change from Baseline to Week 24 (or End of Treatment) in transferrin saturation (TSAT) as measured by blood laboratory tests.
Time frame: Week 24 (or End of Treatment if treated for less than 24 weeks)
Effect of PTG-300 on Serum Iron
Change from Baseline to Week 24 (or End of Treatment) in serum iron as measured by blood laboratory tests.
Time frame: Week 24 (or End of Treatment if treated for less than 24 weeks)
Effect of PTG-300 on Phlebotomy Frequency
Change in number of phlebotomies in 24-weeks before treatment compared with the number of phlebotomies during 24-weeks of treatment with PTG-300.
Time frame: Over 24 weeks
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Protagonist Investigational Site
Conroe, Texas, United States
Protagonist Investigational Site
Dallas, Texas, United States
Protagonist Investigational Site
Houston, Texas, United States
Protagonist Investigational Site
Houston, Texas, United States
Protagonist Investigational Site
Richmond, Virginia, United States
Protagonist Investigational Site
Seattle, Washington, United States
Protagonist Investigational Site
Halifax, Nova Scotia, Canada
...and 1 more locations