
RNAi Drug Developer

Recently, according to the announcement on the CDE official website, Hangzhou Bolin Pharmaceutical Technology Co., Ltd., a subsidiary of Argo, has submitted an application.siRNA Drug "BW-20805 Injection"ObtainClinical Trial Implied Permission(Application No.: CXHL2300824),For the treatment of hereditary angioedema(HAE)。

Source: CDE Official Website
Hereditary Angioedema(HAE)It is a rare and severe autosomal dominant genetic disease characterized by recurrent episodes of self-limiting tissue edema. Currently, there is only one monoclonal antibody drug for this disease available in China — Lanadelumab Injection from Takeda Pharmaceuticals.
BW-20805 is the third siRNA drug approved for clinical trials in China this year by Argo.In addition, the two siRNA drugs previously approved for clinical trials areBW-00163AndBW-00112,Their indications are hypertension and dyslipidemia, respectively.
About Argo
Argo is focused on the development of a new generation of siRNA drugs, with years of professional experience in all aspects of RNAi drug development, including nucleic acid sequence design, chemical modification, GalNAc delivery technology, extrahepatic delivery technology, oligonucleotide synthesis, and CMC.
The company was founded in 2021 by Dr. Dongxu Shu and Dr. Pengcheng Shao, scientists with extensive experience in siRNA drug development.(Previously at well-known companies such as Arrowhead)At its inception, it secured tens of millions in angel round funding from Apricot Capital, followed by an over 400 million yuan A-round financing with investments from multiple well-known institutions.
It is reported that the company currently has several pipelines in the preclinical research stage of new drug application.(IND-enabling)Phase, during which all three drugs have entered Phase 1 clinical trials in China, the U.S., and Australia.
E.N.D

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