2022
Initiated Phase Ⅰ/Ⅱ clinical trial of STP705 in the U.S. for Facial isSCC
Obtained IND clearance from the Taiwan Ministry of Health and Welfare for STP705 in Liver Cancer Treatment
Initiated Phase Ⅰ clinical trial of STP705 in the U.S. for Medical Cosmetology Treatment
Initiated Phase Ⅰ clinical trial of STP707 in the U.S. for Primary sclerosing cholangitis
Initiated Phase Ⅰ clinical trial of STP707 in the U.S. for Solid tumors
2021
Became public on the Main Board of The Stock Exchange of Hong Kong Limited
Established a co-development partnership for STP702 with Walvax
Completed Series E financing, raising approximately US$107 million
Initiated Phase Ⅱb study in the U.S. for STP705 in squamous cell carcinoma in situ
Initiated Phase Ⅱ clinical trial in the U.S. for STP705 for keloid scarless healing
Initiated Phase Ⅰ clinical trial in the U.S. for STP705 for liver cancer
Obtained “acceptance for review” from the NMPA in China for STP705 in squamous cell carcinoma in situ
Obtained IND clearance from the U.S. FDA for STP707
Established a manufacturing facility with fill and finish capacity in Guangzhou, to produce large-scale products with GMP compliance
Started the construction of the southern headquarters of Sirnaomics
2020
Launched RNAimmune, a subsidiary of Sirnaomics
Completed a Series D round of financing, totaling approximately US$104 million
Completed a Phase Ⅰ/Ⅱ study in the U.S. for STP705 in squamous cell carcinoma in situ
Initiated a Phase Ⅱ clinical trial in the U.S. for STP705 in basal cell carcinoma
Sirnaomics Guangzhou obtained the national innovation company certification in China again
2019
Completed a Series C round of financing, totaling US$48 million
Established Sirnaomics Hong Kong
2018
Obtained IND clearance from the U.S. FDA for STP705 in advanced cholangiocarcinoma
Received FDA clearance for Phase Ⅱ study of STP705 for squamous cell carcinoma nonmelanoma skin cancer
2017
Completed a Series B round of financing, totaling US$10 million
Achieved the first IND approval of STP705 for treating hypertrophic scars in China
STP705 granted orphan drug designation by the U.S. FDA for the treatment of Cholangiocarcinoma and primary sclerosing cholangitis
Sirnaomics Guangzhou obtained the national innovation company certification in China
Sirnaomics Guangzhou partnered with Jiangsu Zhengyuan to develop a variety of atomization drug delivery devices
2016
Obtained IND clearance from the U.S. FDA for a Phase Ⅱa clinical study of STP705 in hypertrophic scars
2015
Sirnaomics Suzhou and Sirnaomics Guangzhou were selected as the “Significant New Drug Creation” in the 13th Five-Year Plan for national economic and social development in China
2014
Submitted an IND application to the China Food and Drug Administration for STP705 for the treatment of hypertrophic scars, which would be China's first nucleic acid drug if approved
2013
Sirnaomics Suzhou and Sirnaomics Guangzhou were selected as the “Significant New Drug Creation” in the 12th Five-Year Plan for national economic and social development in China
2012
Expanded presence in China with new offices in Guangzhou, China
Sirnaomics Guangzhou was selected as the Guangzhou Entrepreneurship Leading Talent Project
2009
Sirnaomics’ Suzhou was selected as a Jiangsu Science and Technology Leading Talent Project
Sirnaomics Suzhou was certified as the Suzhou Engineering Research Center for nucleic acid drugs by the Suzhou Science and Technology Bureau
2008
Established Sirnaomics’ China headquarters in Suzhou
2007
Established Sirnaomics’ U.S. headquarters in Gaithersburg, Maryland