3SBio Files For SFDA Approval Of High-Dose EPIAO
3SBio Inc. (NSDQ: SSRX) has filed for SFDA approval of a high-dose, 36,000 IU
formulation of EPIAO for the treatment of anemia resulting from chemotherapy.
Unlike 3SBio’s other formulations of EPO, this one would be exclusive to the
company. A 36,000 IU injection would be administered once every week, a
significant advantage over the three-times per week administration of the more
common 10,000 IU injections.
In its clinical trial, the high-dose EPIAO performed at about the same
levels as the low-dose formulation. In both cases, 70% of the patients
experienced Hemoglobin improvement of 1-2 g/dL from baseline. Safety and
tolerability profiles were also similar. A low grade fever, which disappeared in
time, was the major complaint.
The Phase III trial enrolled 206
non-myeloid malignant tumor patients who were split into two groups: the
once-per week high-dose 36,000 IU patients, and the three-times-per-week 10,000
IU patients. The trial also compared peak Hemoglobin value, nadir Hemoglobin
value and the time required for the Hemoglobin value to increase more than 1
g/dL and 2 g/dL. There was no significant difference between the two groups on
these secondary endpoints.
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