Guangdong Raynovent Biotech Co., Ltd (hereinafter referred to as “Raynovent”), is a sino-foreign joint venture focusing on the research, development and commercialization of innovative drugs in the fields of liver and respiratory diseases. Raynovent was established in October 2018, and headquarters in Guangzhou. It is one subsidiary of Guangdong Zhongsheng Pharmaceutical Co., Ltd, a renowned A-share company(Stock Code: 002317).
On the strength of our remarkable understandings and insights in the pathophysiology of respiratory and liver diseases, we focus on the new treatments R & D for critical diseases such as influenza, avian influenza, idiopathic pulmonary fibrosis (IPF) and non-alcoholic steatohepatitis (NASH). At present, 6 innovative drugs for NASH and respiratory diseases are in pre-clinical or clinical stages. ZSP1601, the first domestic innovative drug approved for clinical trials for NASH, and ZSP1273,the first domestic RNA polymerase inhibitor for influenza A and human avian influenza treatment and prophylaxis have entered into phase 2 clinical trials.
Our vision is to develop and deliver innovative therapies for patients with respiratory and liver diseases, especially viral and infectious diseases, and be a China-leading, World-class, Science-driven innovative biotech company.
Innovation & Excellence
Responsible & Courageous
Teamwork & Integrity
March, 2018 - Commences financing for respiratory and NASH innovative drugs pipeline.
September, 2018 - “Phase 1/2 Clinical Research of Category 1 Drug ZSP1601 for the treatment of Non-Alcoholic Steatohepatitis (NASH)” and “Phase 1/2 Clinical Research of Category 1 Drug ZSP1603 for the treatment of Idiopathic Pulmonary Fibrosis (IPF)” were selected as the Major New Drugs Innovation and Development Scheme by the National Science and Technology Major Projects.
October, 2018 - Established in Dongguan.
December, 2018 - Series A round of financing rasies $15.8 Million by reputable overseas investors, Southern Orchard Limited and Snow Owl, LLC.
March, 2019 - Initiates co-development of the innovative drug RCYM001 for treatment of NASH, with Wuxi AppTec.
March, 2019 - Completes Phase 1 clinical trial of ZSP1601, a first-in-class NASH drug candidate.
March, 2019 - Completes Phase 1 clinical trial of ZSP1273, first RNA rolymerase small molecule inhibitor approved by China for clinical trials.
June, 2019 - Completes Phase 1 clinical trial of ZSP1603, the Category 1 Drug for the treatment of IPF and malignant tumor.
June,2019 - Completes Series A financing of $20Million, with the follow-on funding by overseas investor BioTrack Capital Fund I,LP.
June, 2019 - Signs an agreement to build its headquarter in Futian Bio-Medicine International Industrial Park, Shenzhen-Hong Kong Science and Technology Innovation Cooperation Zone.
August, 2019 - Convenes the National Investigators Conference of Phase 2 clinical trial of ZSP1273 to treat Influenza A, and initiates Phase 2 clinical trial, with Academician Zhong Nanshan as the Principle Investigator (PI).
November, 2019 - ZSP0678, the Category 1 Drug for the treatment of NASH, enteres Phase 1 clinical trial with the dosing of the first patient in China.
November, 2019 - “Development and Research of Category 1 New Chemical Drug WXSH0078 for the treatment of NASH” and “Development and Research of Category 1 New Chemical Drug WXSH0038 for the treatment of NASH” were selected as the Major New Drugs Innovation and Development Scheme by the National Science and Technology Major Projects.
December, 2019 - ZSP1273, the RNA polymerase small molecule inhibitor, enteres Phase 2 clinical trial with the dosing of the first patient in China.