Pharmacokinetic Evaluation of Oral Viscous Budesonide in Paediatric Patients with Eosinophilic Oesophagitis in Repaired Oesophageal Atresia.
Raffaele SimeoliSebastiano A G LavaAlessandro Di DeoMarco RoversiSara CairoliRenato TambucciFrancesca ReaMonica MalamisuraGiulia AngelinoIsabella BiondiAlessandra SimonettiPaola De AngelisCarlo Dionisi-ViciPaolo RossiGiuseppe PontrelliOscar Della PasquaBianca Maria GoffredoPublished in: Pharmaceutics (2024)
Eosinophilic oesophagitis is a long-term complication of oesophageal atresia (EA), an uncommon condition that affects approximately 1 in 3500 infants. An exploratory, open-label phase 2 clinical trial was conducted in paediatric eosinophilic oesophagitis after oesophageal atresia (EoE-EA) to assess the safety, pharmacokinetics, and efficacy of oral viscous budesonide (OVB). In total, eight patients were enrolled in the study and assigned to a twice-daily dosing regimen of either 0.8 or 1 mg OVB, depending on age and height, administered for 12 weeks. OVB was safe and effective in the treatment of EoE-EA. The current investigation focuses on the pharmacokinetics of budesonide and the impact of an oral viscous formulation on its absorption and bioavailability. Using a non-linear mixed effects approach, two distinct absorption profiles were identified, despite marked interindividual variability in drug concentrations. Budesonide exposure was higher than previously reported in children following oral inhalation. Even though no significant effect has been observed on serum cortisol levels, future studies should consider exploring different doses, schedules, and/or treatment durations, as there may be an opportunity to reduce the risk of cortisol suppression.
Keyphrases
- clinical trial
- open label
- intensive care unit
- emergency department
- end stage renal disease
- ejection fraction
- newly diagnosed
- phase ii
- body mass index
- physical activity
- study protocol
- radiation therapy
- squamous cell carcinoma
- peritoneal dialysis
- current status
- phase iii
- double blind
- rectal cancer
- drug induced
- adverse drug
- electronic health record