Publications by authors named "M R Dillingh"

There is a need for antidiabetic agents successfully targeting insulin sensitivity and treating obesity control at the same time. The aim of this first-in-human study was (a) to evaluate safety and tolerability, (b) to evaluate pharmacokinetics and (c) to assess indications of receptor engagement of single ascending doses of KBP-042, a dual amylin and calcitonin receptor agonist (DACRA) that has shown promising preclinical data, with superior activity in terms of typical amylin-induced responses including reduction of food intake, weight loss and gluco-regulatory capacities. A randomised double-blind placebo-controlled single ascending dose study was performed with six dose levels of KBP-042 (5, 7.

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  • The study investigates the effects of low- to moderate-dose endotoxin (LPS) on the endothelium and kidney function in healthy males, focusing on both the magnitude of the response and timing.
  • It was a randomized, double-blind, placebo-controlled trial, where participants received either LPS or a placebo, measuring various inflammatory and kidney injury markers.
  • Results showed significant inflammatory responses with higher LPS doses, but no clinically relevant kidney damage, suggesting this model could be beneficial for future clinical research.
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Background: DNA viruses such as HPV rely on K influx for replication. Both digoxin and furosemide inhibit the K influx by interacting with cell membrane ion co-transporters (Na /K -ATPase and Na -K -2Cl co-transporter-1, respectively). We therefore hypothesized that these two compounds in a topical formulation may be valuable in the treatment of HPV-induced warts.

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  • ONS-3010, developed by Oncobiologics as a biosimilar to Humira, underwent a phase I study to compare its pharmacokinetics, safety, and immunogenicity to both EU and US versions of Humira in healthy volunteers.
  • The study involved 198 participants who received a single dose of either ONS-3010 or Humira, with results showing similar pharmacokinetic profiles and immune responses across treatment groups.
  • Additionally, the research highlighted the effectiveness of ONS-3010 in significantly lowering TNFα levels and interleukin-8 release in response to specific immune challenges, indicating its potential for further clinical development.
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Abnormal fibrogenic repair response upon alveolar injury is believed to play an important role in the pathogenesis of idiopathic pulmonary fibrosis (IPF). PRM-151 (recombinant human pentraxin-2, also known as serum amyloid P), has been shown to reduce fibrosis in preclinical lung fibrosis models, and was well tolerated with a favourable pharmacokinetic profile in an earlier single-dose phase I study.A randomised, double-blind, placebo-controlled, multiple ascending dose trial was performed to assess the tolerability and pharmacokinetic and pharmacodynamic characteristics of multiple doses of PRM-151 in IPF patients.

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