The purpose of the study is to determine tolerability, PK/PD and preliminary efficacy of BPS804 in adult patients with HPP treated with multiple escalating doses of BPS804. This study will allow a comparison of several doses of the study drug within the first two weeks after administration and after a longer assessment period for the highest dose level to enable selection of dose ranges to be tested in subsequent studies in the HPP indication.
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The number (percent) of patients experiencing adverse events or serious adverse events
Timeframe: 141 days following initial investigational product administration
Change from baseline in primary serological bone biomarkers
Timeframe: 141 days following initial investigational product administration