沃尔巴克氏菌
淋巴丝虫病
丝虫病
候选药物
药物发现
医学
药品
药理学
生物
生物信息学
免疫学
生态学
蠕虫
寄主(生物学)
作者
W. David Hong,Paul M. O’Neill,Mark J. Taylor,Joseph D. Turner,Stephen A. Ward,Fabian Gusovsky,Farid Benayoud,Nao Shibuguchi,Dixit Girish,Francis G. Fang,Ravi Kumar Talabhakthla,Anand Vaddi,Chiranjeevi Challa,Karri Satya Ammi Reddy,Vijay Kalla,Sugandham Srinivasa Rao,Durga Mahesh Kumar Nagireddi,Jayesh Patel,Anil Shahaji Khile
标识
DOI:10.1021/acs.oprd.2c00167
摘要
Anti-Wolbachia therapy has been clinically proven to be a safe approach for the treatment of onchocerciasis and lymphatic filariasis. AWZ1066S, a first-in-class highly specific anti-Wolbachia drug candidate developed for a short-course treatment of human filariasis, has advanced into clinical development. An improved, cost-efficient, and scalable process for the manufacture of this clinical candidate is described. Presented herein is the process development work for the active pharmaceutical ingredient (API) and its two key starting materials [2-(trifluoromethyl)-3-pyridyl]methanamine and (S)-3-methylmorpholine, starting from 2,4-dichloropyrido[2,3-d]pyrimidine, which is capable of delivering high-purity (>99%) API consistently. The optimized production route was used in the manufacture of the clinical candidate at the kilogram scale to support the ongoing clinical development.
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