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systematic strategy currently exists to

identify toxicities of therapy for infants

with IH. The consensus team agreed

on a number of recommendations that

arose froma reviewof existing evidence

supplemented by expert opinion and

clinical experience (Table 6). These

recommendations will provide the

platform for large-scale phase II/III

clinical trials to determine optimal

dosing regimens and long-term safety

pro

fi

les. We anticipate that these guide-

lines will be modi

fi

ed as more data

are made available from these future

studies.

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