AI-powered drug discovery and biodefence company Lunai Bioworks (NASDAQ:LNAI) announced on Monday that it has launched a new oncology collaboration with a clinical-stage partner to evaluate data from a randomised Phase 2 metastatic colorectal cancer trial.
The aim is to define biological patient subgroups that are likely to benefit most from the investigational therapy.
Under the pilot agreement, Lunai will deploy its proprietary Augusta AI platform to assess de-identified patient-level clinical, imaging, and longitudinal outcomes data, with a focus on overall survival and disease progression endpoints.
Lunai said that by integrating traditional clinical variables with AI-derived imaging features and temporal response patterns, the company aims to generate data-driven enrichment strategies designed to aid in the FDA trial design, including optimised inclusion criteria, endpoint strategy, and its statistical powering.
The collaboration is starting as a defined pilot project, with potential to expand into a broader commercial multi-study programme as supported by the data. If successful, the partners anticipate exploring additional applications across multiple tumour types, earlier-line treatment settings, and adaptive trial designs such as basket or umbrella studies.
Aptamer Optimer technology integrated into Twist Bioscience TrueAmp Library Preparation Kit
AsymBio builds integrated platforms across biopharmaceutical development lifecycle
Evogene expands Google Cloud collaboration to integrate AI agents into ChemPass AI
Cumulus Neuroscience enters Japanese market with Shionogi collaboration
FDA accepts Takeda's oveporexton NDA with priority review for narcolepsy type 1
Eli Lilly signs definitive agreement to acquire Orna Therapeutics
CiteAb launches new scientific image search tool and improved reagent search engine
Innocan Pharma reports findings from clinical study of LPT-CBD in dogs
Lunai Bioworks starts new oncology collaboration with clinical-stage partner
BioArctic and Eisai secure Priority Review in China for subcutaneous Leqembi
Sanofi's rilzabrutinib receives FDA breakthrough and Japan orphan designations for rare anaemia
Kelun-Biotech reports fourth indication for sac-TMT approved by NMPA in HR+/HER2- breast cancer
Delonix Bioworks gets IND clearance for DX-104 in China
Innovent Biologics collaborates with Eli Lilly to develop new oncology and immunology treatments
Ascentage Pharma receives China IND clearance for BTK degrader APG‑3288