venous irritation
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2020 ◽  
Vol 43 (3) ◽  
pp. 488-492 ◽  
Author(s):  
Shigeru Ishida ◽  
Hanae Morikawa ◽  
Hiroyuki Watanabe ◽  
Toshikazu Tsuji ◽  
Takeshi Sugio ◽  
...  

Author(s):  
Yoshihito Morimoto ◽  
Kumika Miyawaki ◽  
Reisuke Seki ◽  
Kazuhiro Watanabe ◽  
Masayoshi Hirohara ◽  
...  

Author(s):  
Riye Ogawa ◽  
Mitsuyo Ueda ◽  
Nobuaki Egashira ◽  
Shigeru Ishida ◽  
Maki Takeda ◽  
...  

2013 ◽  
Vol 32 (4) ◽  
pp. 274-287 ◽  
Author(s):  
Shayne C. Gad ◽  
Dexter W. Sullivan ◽  
James D. Crapo ◽  
Charles B. Spainhour

Manganese (III) meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin (MnTE-2-PyP or BMX-010; CASRN 219818-60-7) is a manganese porphyrin compound developed as a potential drug substance for use as a radioprotective and for the ex vivo treatment of cells, tissues, and organs intended for transplantation. In preparation for an investigational new drug filing, a full good laboratory practice nonclinical safety assessment was conducted in order to evaluate the safety of MnTE-2-PyP and included the performance of in vitro genotoxicity studies, local tissue tolerance evaluation, safety pharmacology core battery studies, and single- and repeat-dose intravenous (iv) toxicity studies in mice and monkeys. The MnTE-2-PyP was determined not to be genotoxic or hemolytic, did not demonstrate flocculation or elicit adverse pharmacologic effects on respiration, the central nervous system (CNS), and had limited transitory effects on the cardiovascular system only at levels well above the therapeutic target dose. The intended iv clinical solution did not cause venous irritation in rabbits. The no observed adverse effect level (NOAEL) in mice was determined to be 10 mg/kg/day after 18 consecutive days of bolus iv dosing once daily in the morning. The NOAEL in monkeys after 14 days of bolus iv dosing in the morning was determined to be 5 mg/kg/day. At doses relevant to clinical use in humans, neither study revealed any indication of any specific target organ toxicity, including the classic heme porphyrin kidney, liver, CNS, or cardiac toxicities, or manganese toxicity. Mortality seen shortly after dosing in individual animals at higher doses was not accompanied by any organ or clinical pathology indications, suggesting a functional pharmacological-mediated effect. Based on the results of these studies, a conservative safe initial starting clinical dose of 5.0 mg (0.083 mg/kg in a 60 kg adult) was proposed for the initiation of human trials. Because of patent life issues, use of MnTE-2-PyP as a transplantation aid or radioprotective agent is not currently being pursued past the preclinical stages. It serves as a model for the clinical development of this class of drugs.


2013 ◽  
Vol 36 (4) ◽  
pp. 574-578 ◽  
Author(s):  
Hiroyuki Watanabe ◽  
Hiroaki Ikesue ◽  
Tomoko Tsujikawa ◽  
Kenichiro Nagata ◽  
Mayako Uchida ◽  
...  
Keyword(s):  

Author(s):  
Yuri Narishige ◽  
Riye Ogawa ◽  
Yoko Tatsushima ◽  
Shiori Fukui ◽  
Nobuaki Egashira ◽  
...  

2011 ◽  
Vol 20 (7) ◽  
pp. 1549-1553 ◽  
Author(s):  
Takaaki Yamada ◽  
Nobuaki Egashira ◽  
Hiroyuki Watanabe ◽  
Kenichiro Nagata ◽  
Takahisa Yano ◽  
...  

2011 ◽  
Vol 20 (5) ◽  
pp. 951-955 ◽  
Author(s):  
Kenichiro Nagata ◽  
Nobuaki Egashira ◽  
Takaaki Yamada ◽  
Hiroyuki Watanabe ◽  
Yui Yamauchi ◽  
...  

2010 ◽  
Vol 36 (6) ◽  
pp. 698-704
Author(s):  
Chengwen Mao ◽  
Jiangling Wan ◽  
Huabing Chen ◽  
Huibi Xu ◽  
Xiangliang Yang

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