Dose range-finding toxicity study in rats with recombinant human lactoferrin produced inKomagataella phaffii

Author:

Peterson RossORCID,Crawford Robert B.,Blevins Lance K.ORCID,Kaminski Norbert E.ORCID,Sass June S.ORCID,Ferraro BryceORCID,Vishwanath-Deutsch RomaORCID,Clark Anthony J.ORCID,Malinczak Carrie-AnneORCID

Abstract

ABSTRACTThe oral toxicity of recombinant human lactoferrin (Helaina rhLF, Effera™) produced inKomagataella phaffiiwas investigated in adult Sprague-Dawley rats by once daily oral gavage for 14 consecutive days. The study used groups of 3-6 rats/sex/dose. The vehicle control group received sodium citrate buffer and the test groups received daily doses of 200, 1000 and 2000 mg of rhLF per kg body weight. Bovine LF at 2000 mg/kg body weight per day was used as a comparative control. Clinical observations, body weight, hematology, clinical chemistry, iron parameters, immunophenotyping, and gross examination at necropsy were used as criteria for detecting the effects of treatment in all groups and to inform dose levels for future toxicology studies. Quantitative LF levels were also analyzed as an indication of bioavailability. Overall, administration of Helaina rhLF by once daily oral gavage for 14 days was well tolerated in rats at levels up to 2000 mg/kg/day, or 400x Helaina’s intended commercial use, and indicating that a high dose of 2000 mg/kg/day is appropriate for future definitive toxicology studies.

Publisher

Cold Spring Harbor Laboratory

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