Pharmaceutical company TaiwanJ Pharmaceuticals reported on Monday the launch of a USD26m contract to license out its drug candidate JKB-122 to Newsoara Biopharma for further development in Asia.
JKB-122, TaiwanJ's effective phase 2 nonalcoholic fatty liver disease (NAFLD)/nonalcoholic steatohepatitis (NASH) drug candidate, had been licensed out to Newsoara Biopharma Co Ltd, based in Shanghai. JKB-122 is a small molecule and a long-acting TLR4 antagonist showing anti-fibrotic, immuno-modulating, and anti-inflammatory effects for the treatments of Non-Alcoholic Fatty Liver Disease (NAFLD), Autoimmune Hepatitis (AIH) and Non-Alcoholic Steatohepatitis (NASH).
A drug development company, Newsoara Biopharma will be responsible for the clinical development and market commercialisation of JKB-122 in Asia, except Taiwan.
Under the terms of the agreement, TaiwanJ will receive USD2m of upfront as well as up to USD24m of milestone payments, which will be paid when each milestone in the development and commercialisation process is achieved.
The partnership will conduct preclinical research for JKB-122's second generation compound JKB-133.
In conjunction with the agreement, TaiwanJ will maintain its right of global clinical development and subsequent worldwide market commercialisation.
Chemomab secures new patents for CM-101 monoclonal antibody
argenx receives FDA priority review for VYVGART Hytrulo in CIDP
Diamyd Medical granted US FDA Fast Track designation for Diamyd diabetes treatment
Ono partners with Shattuck Labs for bifunctional fusion proteins
Artax Biopharma doses first subject in AX-158 Phase 2a psoriasis trial
Innovent Biologics announces CFO transition
Bio-Thera Solutions commences dosing in BAT6026 Phase IA/IIB clinical trial
BioSenic expands patent coverage for ATO therapeutic platform
Celltrion USA submits CT-P47 Biologics License Application to FDA
NS Pharma's NS-229 receives European Commission orphan drug designation
Kyverna Therapeutics' KYV-101 granted US FDA fast track designation
InnoCare Pharma receives U.S. FDA clearance for ICP-248 clinical trial