The purpose of this study is to evaluate the extent of moxidectin transfer into the breast milk of lactating women and to provide the initial pharmacokinetic and safety profile of moxidectin in lactating women.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Masking
NONE
Enrollment
12
Unnamed facility
Plymouth, United Kingdom
Blood samples
Time frame: 4 months
Safety based on adverse event monitoring, vital sign measurements, 12-lead ECGs and routine lab tests.
Time frame: 4 months
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