Insilico Medicine (HK:3696), a clinical-stage drug discovery and development company driven by generative artificial intelligence (AI), announced on Friday that ISM8969, an orally available NLRP3 inhibitor targeting inflammation and neurodegenerative disorders, has received investigational new drug (IND) clearance from the US Food and Drug Administration (FDA) for the treatment of Parkinson's Disease.
The Phase I clinical trial plans to evaluate the safety, tolerability, and pharmacokinetics of ISM8969 in healthy volunteers, and to identify the optimal dose level(s) to be recommended for further investigation.
ISM8969 was discovered and optimised using Insilico's Chemistry42, a comprehensive generative chemistry engine consisting of multiple applications across the drug design and discovery stages.
To accelerate the global development of ISM8969, Insilico Medicine has entered into a co-development collaboration agreement which grants Hygtia Therapeutics worldwide rights to research, develop, register, manufacture, and commercialise ISM8969, with both parties each holding 50% of the global rights and interests to the programme. In return, Insilico is eligible to receive up to USD66m in upfront and milestone payments.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA