Reported impact
Business outcome
Novartis aims to reduce drug discovery and development timelines, improve decision quality, surface risks earlier, shorten iterative cycles, and help teams bring therapies to patients faster with a higher likelihood of success.
- Productivity Improvement
- Risk Reduction
- Speed to Market
Solution
Novartis describes an in-house, AI-enabled R&D decision-support approach that spans research, preclinical work, clinical development, and documentation. Data is ingested from human genetic and multi-omic datasets, imaging, clinical trial results, decades of published research, real-world evidence, protein information, prior chemistry, and clinical and operational study data. AI models are used to integrate these sources for target identification and validation, while generative chemistry methods explore molecular design spaces and optimize multiple properties in parallel. In development, Generative AI paired with knowledge graphs summarizes prior studies and evidence to support protocol drafting, and trial computational twins simulate what-if clinical design scenarios. AI-enhanced analytics monitor supply, recruitment, and study risks and recommend next best actions. The article does not name a storage platform, but it does describe approved-source workflows, privacy and quality controls, and expert human review before outputs are used in regulated R&D decisions.
Data flow
Novartis feeds genetic, multi-omic, imaging, trial, literature, real-world, protein, chemistry, clinical, and operational data into AI models and analytics. Those models generate target insights, molecule proposals, safety signals, protocol summaries, trial simulations, and study-risk recommendations, which are then reviewed by Novartis scientists and clinicians to guide R&D, trial design, and regulatory documentation.