Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Hiroyoshi Kakuyama"'
Autor:
Naoto Noda, Takeshi Takagaki, Yasuhide Yodo, Yuzo Horibuchi, Shuichi Iino, Shunji Matsuki, Yoichiro Ogama, Hiroyoshi Kakuyama
Publikováno v:
Pharmacology Research & Perspectives, Vol 9, Iss 5, Pp n/a-n/a (2021)
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
Externí odkaz:
https://doaj.org/article/b804592a5ce74d749d7cb7315b7cacf7
Publikováno v:
The Journal of Clinical Pharmacology.
Autor:
Yoshiko Tomita, Takeshi Takagaki, Hiroyoshi Kakuyama, Hironori Nishibe, Daisuke Nemoto, Atsushi Kitamura
Publikováno v:
The Journal of Clinical Pharmacology. 61:1069-1080
Blonanserin is an atypical antipsychotic drug with high affinity and selective antagonism for dopamine D2 and D3 and serotonin 5-HT2A receptors. Blonanserin transdermal patch is the first transdermal formulation developed for the treatment of schizop
Autor:
Naoyuki Sawada, Yosuke Nakada, Takeshi Takagaki, Yuta Shibue, Hiroyoshi Kakuyama, Tatsuto Hamatani, Masayo Hashimoto
Publikováno v:
Drug Metabolism and Pharmacokinetics. 35:563-570
Minesapride is a novel 5-hydroxytryptamine 4 (5-HT4) receptor partial agonist that is expected to show efficacy in patients with irritable bowel syndrome with predominant constipation and functional constipation. An open-label study was conducted to
Autor:
Takeshi Sakayori, Hironori Nishibe, WooChan Kim, Amane Tateno, Masahiro Yamamoto, Hiroyoshi Kakuyama, Yoshiro Okubo
Publikováno v:
International Journal of Neuropsychopharmacology
Background Transdermal antipsychotic patch formulations offer potential benefits, including improved adherence. This study investigated the striatal dopamine D2 receptor occupancy with daily blonanserin transdermal patch application. Methods This ope
Publikováno v:
Clinical Pharmacology in Drug Development. 9:353-365
We hypothesized that DSP-6952, a partial agonist of the 5-hydroxytryptamine type-4 receptor and a gastrointestinal prokinetic agent, can induce natural bowel movements by enhancing gastrointestinal motility and colonic transit in patients with chroni
Autor:
Naoto Noda, Tatsuto Hamatani, Yuta Shibue, Takeshi Takagaki, Atsushi Kitamura, Miwa Haranaka, Yoichiro Ogama, Hiroyoshi Kakuyama
Publikováno v:
Clinical pharmacology in drug developmentReferences. 11(10)
EPI-589 attenuates oxidative stress due to the radical scavenging activity of the reduced form and affects mitochondrial energy metabolism as a substrate of quinone-oxidoreductases. Given the effects of EPI-589 on oxidative stress and mitochondrial d
Autor:
Atsushi, Kitamura, Takeshi, Takagaki, Daisuke, Nemoto, Yoshiko, Tomita, Hironori, Nishibe, Hiroyoshi, Kakuyama
Publikováno v:
Journal of clinical pharmacologyReferences. 61(8)
Blonanserin is an atypical antipsychotic drug with high affinity and selective antagonism for dopamine D
Autor:
Tatsuto, Hamatani, Yuta, Shibue, Naoyuki, Sawada, Takeshi, Takagaki, Masayo, Hashimoto, Yosuke, Nakada, Hiroyoshi, Kakuyama
Publikováno v:
Drug metabolism and pharmacokinetics. 35(6)
Minesapride is a novel 5-hydroxytryptamine 4 (5-HT
Autor:
Takeshi Takagaki, Minoru Itou, Naoki Uchida, Kazuaki Inoue, Daisuke Ishii, Tomoe Fujita, Hiroyoshi Kakuyama
Publikováno v:
Journal of clinical pharmacologyReferences. 60(10)
Ranirestat is an aldose reductase inhibitor hypothesized to improve diabetic neuropathy. An open-label, single-dose, parallel-group study was conducted to compare pharmacokinetic (PK) characteristics of an oral dose of ranirestat across subjects with