This study will assess the safety and efficacy of multiple-dose of STSP-0601 for the treatment of bleeding episodes in hemophilia A or B patients with inhibitors.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
77
A multiple-dose design to evaluate the safety,tolerability and efficacy of two doses of STSP-0601 for injection in patients with inhibitory hemophilia
A multiple-dose design to evaluate the safety,tolerability and efficacy of two doses of STSP-0601 for injection in patients with inhibitory hemophilia
Hospital of Hematology, Chinese Academy of Medical Sciences
Tianjin, Tianjin Municipality, China
Incidence of adverse events
Time frame: From day 0 to up to day 8
Proportion of successfully treated bleeding episodes
Time frame: 24 hours after administration of study drug
Proportion of bleeding episodes with clinical relief of signs and symptoms
Time frame: 4 hours、8 hours、24 hours after first administration of study drug
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