Minimum Effective Dose of Clemastine in a Mouse Model of Preterm White Matter Injury.
Elizabeth OdellNora JabassiniBjörn SchniedewindSarah E Pease-RaissiAdam FrymoyerUwe ChristiansAri J GreenJonah R ChanBridget Elaine LaMonica OstremPublished in: bioRxiv : the preprint server for biology (2024)
Preterm white matter injury (PWMI) is the most common cause of brain injury and cerebral palsy in premature neonates.Clemastine, an FDA-approved antihistamine, was recently identified to strongly promote myelination in a mouse model of PWMI and is a possible treatment.The minimum effective dose in neonatal rodents is unknown and is critical for guiding dose selection and balancing efficacy with toxicity in future clinical trials.We identified the minimum effective dose of clemastine and the associated pharmacokinetics in a murine chronic hypoxia model of PWMI, paving the way for a future clinical trial in human neonates.