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.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval