Normal Neurodevelopment and Fertility in Juvenile Male Rats Exposed to Polyethylene Glycol Following Dosing With PEGylated rFIX (Nonacog Beta Pegol, N9-GP): Evidence from a 10-Week Repeat-Dose Toxicity Study

Author:

Jensen Vivi F. H.1ORCID,Schefe Line H.2,Jacobsen Helene2,Mølck Anne-Marie1,Almholt Kasper1ORCID,Sjögren Ingrid1,Dalsgaard Charlotte M.1,Kirk Rikke K1,Benie Andrew J.3ORCID,Petersen Bent O.3,Kyhn Mette S.4,Overgaard Anne J.4,Bjørnsdottir Inga2,Stannard Diane R.5,Offenberg Hanne K.2,Egecioglu Emil2

Affiliation:

1. Department of Safety Sciences & Imaging, Novo Nordisk A/S, Måløv, Denmark

2. Department of DMPK (Drug Metabolism and Pharmacokinetics) and Non-clinical Project Management, Novo Nordisk A/S, Måløv, Denmark

3. Department of Biophysics & Formulation 1, Novo Nordisk A/S, Måløv, Denmark

4. Department of Non-clinical and Clinical Assay Sciences, Novo Nordisk A/S, Måløv, Denmark

5. Labcorp Early Development Laboratories Limited, Eye, UK

Abstract

N9-GP/Rebinyn®/Refixia® is an approved PEGylated (polyethylene glycol-conjugated) recombinant human factor IX intended for prophylactic and/or on-demand treatment in adults and children with haemophilia B. A juvenile neurotoxicity study was conducted in male rats to evaluate effects on neurodevelopment, sexual maturation, and fertility following repeat-dosing of N9-GP. Male rats were dosed twice weekly from Day 21 of age with N9-GP or vehicle for 10 weeks, followed by a dosing-free recovery period for 13 weeks and terminated throughout the dosing and recovery periods. Overall, dosing N9-GP to juvenile rats did not result in any functional or pathological effects, as measured by neurobehavioural/neurocognitive tests, including motor activity, sensory function, learning and memory as well as growth, sexual maturation, and fertility. This was further supported by the extensive histopathologic evaluation of brain tissue. Exposure and distribution of polyethylene glycol was investigated in plasma, choroid plexus, cerebrospinal fluid, and brain sections. PEG did not cross the blood brain barrier and PEG exposure did not result in any effects on neurodevelopment. In conclusion, dosing of N9-GP to juvenile rats did not identify any effects on growth, sexual maturation and fertility, clinical and histological pathology, or neurodevelopment related to PEG exposure and supports the prophylactic use of N9-GP in children.

Publisher

SAGE Publications

Subject

Toxicology

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