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A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis

OX40 plays an essential role in maintaining late T‐cell proliferation and survival by suppressing apoptosis and by inducing T‐cell memory formation. Here, we report the results of the phase 1 study of KHK4083, a fully human antimonoclonal antibody specific for OX40. In this study, we aimed to assess...

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Autores principales: Furihata, Kenichi, Ishiguro, Yoh, Yoshimura, Naoki, Ito, Hiroaki, Katsushima, Shinji, Kaneko, Etsuji, Shimabe, Munetake, Mukai, Mayumi, Watanabe, Risa, Morishige, Takuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8451804/
https://www.ncbi.nlm.nih.gov/pubmed/33512065
http://dx.doi.org/10.1002/cpdd.918
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author Furihata, Kenichi
Ishiguro, Yoh
Yoshimura, Naoki
Ito, Hiroaki
Katsushima, Shinji
Kaneko, Etsuji
Shimabe, Munetake
Mukai, Mayumi
Watanabe, Risa
Morishige, Takuya
author_facet Furihata, Kenichi
Ishiguro, Yoh
Yoshimura, Naoki
Ito, Hiroaki
Katsushima, Shinji
Kaneko, Etsuji
Shimabe, Munetake
Mukai, Mayumi
Watanabe, Risa
Morishige, Takuya
author_sort Furihata, Kenichi
collection PubMed
description OX40 plays an essential role in maintaining late T‐cell proliferation and survival by suppressing apoptosis and by inducing T‐cell memory formation. Here, we report the results of the phase 1 study of KHK4083, a fully human antimonoclonal antibody specific for OX40. In this study, we aimed to assess the safety and tolerability of a single intravenous or subcutaneous administration of KHK4083 compared with placebo in healthy Japanese and Caucasian subjects and determined the pharmacokinetics (PK) and immunogenicity. Also, we assessed the preliminary efficacy and pharmacodynamics of multiple intravenous doses in Japanese patients with moderate to severe ulcerative colitis (UC). Drug‐related treatment emergent adverse events occurred in 21 healthy subjects (58.3%) and 5 patients with UC (62.5%) after administration of KHK4083. There were no serious adverse events. The PK profile of a single intravenous dose of 10 mg/kg KHK4083 was similar in healthy Japanese and Caucasian subjects. Of 8 UC patients, a clinical response was observed in 3 patients (37.5%) and clinical remission in 2 patients (25.0%) in week 6. Our study demonstrated the safety and tolerability of single and multiple administrations of KHK4083 in healthy Japanese and Caucasian subjects and Japanese patients with moderate to severe UC. It also indicated favorable pharmacological properties of the drug.
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spelling pubmed-84518042021-09-27 A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis Furihata, Kenichi Ishiguro, Yoh Yoshimura, Naoki Ito, Hiroaki Katsushima, Shinji Kaneko, Etsuji Shimabe, Munetake Mukai, Mayumi Watanabe, Risa Morishige, Takuya Clin Pharmacol Drug Dev Articles OX40 plays an essential role in maintaining late T‐cell proliferation and survival by suppressing apoptosis and by inducing T‐cell memory formation. Here, we report the results of the phase 1 study of KHK4083, a fully human antimonoclonal antibody specific for OX40. In this study, we aimed to assess the safety and tolerability of a single intravenous or subcutaneous administration of KHK4083 compared with placebo in healthy Japanese and Caucasian subjects and determined the pharmacokinetics (PK) and immunogenicity. Also, we assessed the preliminary efficacy and pharmacodynamics of multiple intravenous doses in Japanese patients with moderate to severe ulcerative colitis (UC). Drug‐related treatment emergent adverse events occurred in 21 healthy subjects (58.3%) and 5 patients with UC (62.5%) after administration of KHK4083. There were no serious adverse events. The PK profile of a single intravenous dose of 10 mg/kg KHK4083 was similar in healthy Japanese and Caucasian subjects. Of 8 UC patients, a clinical response was observed in 3 patients (37.5%) and clinical remission in 2 patients (25.0%) in week 6. Our study demonstrated the safety and tolerability of single and multiple administrations of KHK4083 in healthy Japanese and Caucasian subjects and Japanese patients with moderate to severe UC. It also indicated favorable pharmacological properties of the drug. John Wiley and Sons Inc. 2021-01-29 2021-08 /pmc/articles/PMC8451804/ /pubmed/33512065 http://dx.doi.org/10.1002/cpdd.918 Text en © 2021 The Authors. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Furihata, Kenichi
Ishiguro, Yoh
Yoshimura, Naoki
Ito, Hiroaki
Katsushima, Shinji
Kaneko, Etsuji
Shimabe, Munetake
Mukai, Mayumi
Watanabe, Risa
Morishige, Takuya
A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis
title A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis
title_full A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis
title_fullStr A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis
title_full_unstemmed A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis
title_short A Phase 1 Study of KHK4083: A Single‐Blind, Randomized, Placebo‐Controlled Single‐Ascending‐Dose Study in Healthy Adults and an Open‐Label Multiple‐Dose Study in Patients With Ulcerative Colitis
title_sort phase 1 study of khk4083: a single‐blind, randomized, placebo‐controlled single‐ascending‐dose study in healthy adults and an open‐label multiple‐dose study in patients with ulcerative colitis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8451804/
https://www.ncbi.nlm.nih.gov/pubmed/33512065
http://dx.doi.org/10.1002/cpdd.918
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