Publications by authors named "Tomohiro Onoue"

This study estimated the incidence of moderate-to-severe drug-induced interstitial lung disease (ILD) among patients with breast cancer in Japan. We analyzed a large nationwide database of patients with breast cancer treated with anticancer therapies between 2009 and 2022. ILD was identified using diagnostic codes and treatment records.

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Article Synopsis
  • - Daprodustat is an oral medication being compared to darbepoetin alfa (an existing treatment) for its effectiveness in treating anemia in Japanese patients undergoing hemodialysis due to chronic kidney disease (CKD).
  • - The study, a phase 3 randomized trial, found that daprodustat maintained hemoglobin levels similarly to darbepoetin alfa, showing it to be noninferior, meaning it is just as effective.
  • - Additionally, daprodustat demonstrated a greater decrease in hepcidin levels and an increase in total iron-binding capacity, suggesting enhanced iron metabolism compared to darbepoetin alfa, with most participants experiencing similar rates of side effects.
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Article Synopsis
  • - Daprodustat is a drug that helps stimulate red blood cell production (erythropoiesis) by mimicking the body's response to low oxygen levels, making it a potential treatment for anemia related to chronic kidney disease (CKD).
  • - A study involving 64 healthy Japanese males tested two different tablet strengths of daprodustat to check if they were bioequivalent and how food impacted its absorption in the body.
  • - Results showed that the 2-mg and 4-mg daprodustat tablets were bioequivalent, and eating a standard meal did not significantly affect how the drug was processed in the body, with the drug being well tolerated among participants.
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Article Synopsis
  • Daprodustat is an oral medication aimed at treating anemia in patients with chronic kidney disease, specifically focusing on those undergoing hemodialysis and not using erythropoiesis-stimulating agents.
  • In a 24-week clinical trial, 28 Japanese patients were given daprodustat starting at 4 mg daily, which successfully raised their hemoglobin levels from a baseline of 9.10 g/dL to the target range of 10.0 to 12.0 g/dL by week 8.
  • Throughout the study, daprodustat maintained these hemoglobin levels without introducing any new safety issues among the participants.
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We developed a pravastatin derivative, sodium (3R,5R)-3,5-dihydroxy-7-((1S,2S,6S,8S)-6-hydroxy-2-methyl-8-((1-[(11)C]-(E)-2-methyl-but-2-enoyl)oxy)-1,2,6,7,8,8a-hexahydronaphthalen-1-yl)heptanoate ([(11)C]DPV), as a positron emission tomography (PET) probe for noninvasive measurement of hepatobiliary transport, and conducted pharmacokinetic analysis in rats as a feasibility study for future clinical study. Transport activities of DPV in freshly isolated rat hepatocytes and rodent multidrug resistance-associated protein 2 (rMrp2; human, MRP2)-expressing membrane vesicles were similar to those of pravastatin. Rifampicin diminished the uptake of DPV and pravastatin by the hepatocytes, with similar inhibition potency.

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