Insilico Medicine, a biotechnology company based in New York and Hong Kong, has developed an AI-designed drug, ISM018_055, targeting idiopathic pulmonary fibrosis, a fatal lung disease. The drug has entered Phase II clinical trials, marking a milestone in drug discovery. Insilico utilized AI throughout the drug’s development process with their Pharma.AI platform, significantly accelerating the traditional drug discovery timeline.
The drug showed promising results in reducing scarring in cells and animal models in Phase I trials, which were successfully completed last year in healthy volunteers. The team recently published their innovative approach in Nature Biotechnology and launched Phase II trials to further test the drug’s safety and efficacy in patients with the disease.
Traditionally, drug discovery involves a lengthy and costly process with a high failure rate. Insilico’s AI-driven approach aims to revolutionize this process by identifying novel targets and designing new molecules more efficiently. The company’s AI platform successfully identified a target and expedited the drug discovery process, validating the effectiveness of AI in drug development.
Insilico’s AI scientists, such as PandaOmics and Chemistry42, played crucial roles in identifying potential targets and designing the drug candidate. With the success of ISM018_055 thus far, Insilico is paving the way for the future of AI-driven drug discovery. Dr. Michael Levitt, a Nobel laureate in chemistry, commended Insilico’s achievement, highlighting the significance of their accelerated drug discovery process.