Publications by authors named "J Oosterhaven"

Bruton's tyrosine kinase (BTK) is a potential therapeutic target for allergic and autoimmune diseases. This first-in-human phase I study evaluated safety, pharmacokinetic, and pharmacodynamic profiles of sofnobrutinib (formerly AS-0871), a highly selective, orally available, non-covalent BTK inhibitor, in healthy adult subjects. Single ascending doses (SAD; 5-900 mg) and multiple ascending doses (MAD; 50-300 mg twice daily [b.

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Background: The Recap of atopic eczema questionnaire (RECAP) was developed to measure eczema control in patients with atopic dermatitis (AD). The measurement properties of RECAP have not yet been validated in caregivers of children with AD.

Objectives: To assess the construct validity, responsiveness, reliability and interpretability of the Dutch proxy version of RECAP.

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Introduction: Pain neuroscience education is part of interdisciplinary pain management programs (IPMPs). To date, the role of health literacy on patients' understanding of pain neuroscience education has not sufficiently been examined.

Objectives: Drawing on interviews with patients with diverse levels of health literacy, this article explores patient perspectives on pain neuroscience education.

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Article Synopsis
  • Limited research has been conducted on the validity and reliability of the Recap of atopic eczema (RECAP) questionnaire, particularly its interpretability for adults with atopic dermatitis (AD).
  • A study involving 200 adult participants aimed to assess the validity, reliability, and responsiveness of the Dutch RECAP by collecting data at multiple time points and comparing results with established reference instruments.
  • The findings indicated that 82% of hypotheses regarding single-score validity were confirmed, and the RECAP effectively differentiated between varying degrees of disease severity, with established score bands to interpret eczema control levels.
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EDP-297 is a farnesoid X receptor agonist under development for treating nonalcoholic steatohepatitis. The pharmacokinetic (PK), pharmacodynamic (PD), food effect, and safety were evaluated in a single ascending dose (SAD) and multiple ascending dose (MAD) phase I study. Healthy subjects received single EDP-297 doses of 20-600 μg or once daily doses of 5-90 μg for 14 days.

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