LG Chem licensed LG00303174 (TT-01025) from TransThera Biosciences Co. Ltd, a clinical-stage biotechnology company based in Nanjing, China.
LG Chem had entered into an exclusive license agreement with TransThera in August 2020 to research, develop, manufacture, and commercialize LG00303174 in the world except China and Japan.
According to the company, LG00303174 is a potential best-in-class novel SSAO/VAP-1 inhibitor, currently being developed for the treatment of chronic inflammatory diseases, including non-alcoholic steatohepatitis. The phase 1 study is currently being conducted within the US and approximately 64 subjects are expected to be enrolled.
LG Chem Life Sciences is a business division within LG Chem, engaged in the development, manufacturing, as well as commercializing pharmaceutical products globally.
LG Chem Life Sciences seeks to expand and make global presence by focusing on key core therapeutic areas of Immunology, Oncology, and Metabolic Diseases (specifically, diabetes and related metabolic diseases). To achieve such, its strategy is to actively pursue global collaboration encompassing from asset-centric to strategic investment and collaboration.
TransThera Biosciences is a clinical-stage biotechnology company focused on developing innovative therapeutics to target diseases with major unmet medical needs via internal research platform and open innovation.
TransThera's current portfolio covers therapeutic areas such as oncology, cardiovascular, and inflammatory diseases.
Innovent and Ollin Biosciences report IBI324 study data in wAMD and DME
Boston Scientific receives FDA clearance for Asurys fluid management system
Lilly presents Phase 3b Taltz (ixekizumab) plus Zepbound (tirzepatide) data at AAD Annual Meeting
Hoth Therapeutics deploys OpenClaw AI platform for drug discovery
Thermo Fisher Scientific and SHL Medical launch integrated US drug-device manufacturing
Bambusa Therapeutics names new CFO
Mabtech partners with Sai Life Sciences to expand access to EYRA multiplex immunology platform
Vimgreen Pharmaceuticals receives IND clearance for VG081821 in China
Inimmune reports dosing of first patient in Phase 2 allergen challenge chamber trial of INI-2004
Gesynta Pharma doses first patient in vipoglanstat Phase 2 clinical proof-of-concept trial
Immunic granted European patent for vidofludimus calcium dosing regimens
Biofrontera reports Phase 2b data for Ameluz photodynamic therapy in acne vulgaris treatment