Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteers

Abstract This study examined the safety, tolerability, and pharmacokinetics (PK) of napabucasin in healthy Asian and non‐Asian participants and investigated the potential for QT/QTc interval prolongation. This five‐part (A–E) study proceeded in a stepwise manner, unless stopping criteria were met. P...

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Main Authors: Naoto Noda, Takeshi Takagaki, Yasuhide Yodo, Yuzo Horibuchi, Shuichi Iino, Shunji Matsuki, Yoichiro Ogama, Hiroyoshi Kakuyama
Format: Article
Language:English
Published: Wiley 2021-10-01
Series:Pharmacology Research & Perspectives
Subjects:
Online Access:https://doi.org/10.1002/prp2.874
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spelling doaj-b804592a5ce74d749d7cb7315b7cacf72021-10-11T10:00:37ZengWileyPharmacology Research & Perspectives2052-17072021-10-0195n/an/a10.1002/prp2.874Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteersNaoto Noda0Takeshi Takagaki1Yasuhide Yodo2Yuzo Horibuchi3Shuichi Iino4Shunji Matsuki5Yoichiro Ogama6Hiroyoshi Kakuyama7Clinical Research Drug Development Division Sumitomo Dainippon Pharma Co., Ltd. Tokyo JapanClinical Research Drug Development Division Sumitomo Dainippon Pharma Co., Ltd. Osaka JapanData Science Drug Development Division Sumitomo Dainippon Pharma Co., Ltd. Tokyo JapanOncology Clinical Development Unit Sumitomo Dainippon Pharma Co., Ltd. Tokyo JapanOncology Clinical Development Unit Sumitomo Dainippon Pharma Co., Ltd. Tokyo JapanFukuoka Mirai Hospital SOUSEIKAI Fukuoka JapanSumida Hospital SOUSEIKAI Tokyo JapanClinical Research Drug Development Division Sumitomo Dainippon Pharma Co., Ltd. Tokyo JapanAbstract This study examined the safety, tolerability, and pharmacokinetics (PK) of napabucasin in healthy Asian and non‐Asian participants and investigated the potential for QT/QTc interval prolongation. This five‐part (A–E) study proceeded in a stepwise manner, unless stopping criteria were met. Parts A–D were randomized, double‐blind, placebo‐controlled, and included healthy Asian male and female and non‐Asian male participants. PK parameters were measured following single‐dose napabucasin (80–1200 mg) in the fasted or fed state (Part D). Potential QT/QTc interval prolongation was assessed using digital 12‐lead electrocardiogram (Parts B and C). Part E was open‐label, and examined the PK of single‐dose napabucasin (240–720 mg) in healthy non‐Asian males. Safety and tolerability were measured in Parts A–E. Changes from baseline in the Fridericia‐corrected QT interval (ΔQTcF) and other electrocardiogram parameters were analyzed using a linear mixed‐effects model. Napabucasin was well‐tolerated across the study (n = 70), and no serious adverse events or significant safety issues were reported when administered with or without food. The most frequent treatment‐emergent adverse events were diarrhea and abdominal pain, and these were mild in severity. No prolongation of the QTcF interval was reported following single‐dose napabucasin (240–1200 mg) and changes in other cardiac parameters were negligible. The PK profile of napabucasin was consistent with earlier studies. Single‐dose napabucasin was tolerated in healthy male and female participants, and no significant safety (including no QTcF prolongation) or tolerability issues were identified, irrespective of food intake. Clinical studies of napabucasin in advanced cancers are ongoing.https://doi.org/10.1002/prp2.874Asianhealthy volunteersnapabucasinnon‐AsianpharmacokineticsQT/QTc interval
collection DOAJ
language English
format Article
sources DOAJ
author Naoto Noda
Takeshi Takagaki
Yasuhide Yodo
Yuzo Horibuchi
Shuichi Iino
Shunji Matsuki
Yoichiro Ogama
Hiroyoshi Kakuyama
spellingShingle Naoto Noda
Takeshi Takagaki
Yasuhide Yodo
Yuzo Horibuchi
Shuichi Iino
Shunji Matsuki
Yoichiro Ogama
Hiroyoshi Kakuyama
Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteers
Pharmacology Research & Perspectives
Asian
healthy volunteers
napabucasin
non‐Asian
pharmacokinetics
QT/QTc interval
author_facet Naoto Noda
Takeshi Takagaki
Yasuhide Yodo
Yuzo Horibuchi
Shuichi Iino
Shunji Matsuki
Yoichiro Ogama
Hiroyoshi Kakuyama
author_sort Naoto Noda
title Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteers
title_short Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteers
title_full Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteers
title_fullStr Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteers
title_full_unstemmed Effects of a reactive oxygen species generator, napabucasin (BBI608), on tolerability, safety, pharmacokinetics, and QT/QTc interval in healthy volunteers
title_sort effects of a reactive oxygen species generator, napabucasin (bbi608), on tolerability, safety, pharmacokinetics, and qt/qtc interval in healthy volunteers
publisher Wiley
series Pharmacology Research & Perspectives
issn 2052-1707
publishDate 2021-10-01
description Abstract This study examined the safety, tolerability, and pharmacokinetics (PK) of napabucasin in healthy Asian and non‐Asian participants and investigated the potential for QT/QTc interval prolongation. This five‐part (A–E) study proceeded in a stepwise manner, unless stopping criteria were met. Parts A–D were randomized, double‐blind, placebo‐controlled, and included healthy Asian male and female and non‐Asian male participants. PK parameters were measured following single‐dose napabucasin (80–1200 mg) in the fasted or fed state (Part D). Potential QT/QTc interval prolongation was assessed using digital 12‐lead electrocardiogram (Parts B and C). Part E was open‐label, and examined the PK of single‐dose napabucasin (240–720 mg) in healthy non‐Asian males. Safety and tolerability were measured in Parts A–E. Changes from baseline in the Fridericia‐corrected QT interval (ΔQTcF) and other electrocardiogram parameters were analyzed using a linear mixed‐effects model. Napabucasin was well‐tolerated across the study (n = 70), and no serious adverse events or significant safety issues were reported when administered with or without food. The most frequent treatment‐emergent adverse events were diarrhea and abdominal pain, and these were mild in severity. No prolongation of the QTcF interval was reported following single‐dose napabucasin (240–1200 mg) and changes in other cardiac parameters were negligible. The PK profile of napabucasin was consistent with earlier studies. Single‐dose napabucasin was tolerated in healthy male and female participants, and no significant safety (including no QTcF prolongation) or tolerability issues were identified, irrespective of food intake. Clinical studies of napabucasin in advanced cancers are ongoing.
topic Asian
healthy volunteers
napabucasin
non‐Asian
pharmacokinetics
QT/QTc interval
url https://doi.org/10.1002/prp2.874
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