XtalPi发布Kodexia闭环siRNA发现平台
XtalPi(晶泰科技)10月6日公布其闭环平台 Kodexia,称将生成式AI、生物建模与自动化实验结合以加速siRNA药物发现,并披露六个覆盖代谢、肾脏、呼吸和中枢神经系统疾病的专有临床前项目,其中过半已完成动物药效测试。平台核心为自研 siFormer 架构,据公司称内部临床前基准显示分子设计效率接近传统流程的三倍,多个项目首轮设计中有超过50%的体内活性优于阳性对照。公司还称其 IgA 肾病先导项目在7个月内取得非人灵长类药效数据,活性与持久性优于同靶点临床阶段参照分子,但这些均属公司自报结果。
若这些自报数据成立,Kodexia 展示了把设计、测试与递送优化连成闭环的AI药物发现路径,但肝外递送与人体验证仍是关键门槛。
XtalPi has outlined how Kodexia, its closed-loop platform, combines generative AI, biological modeling and automated experiments to accelerate the discovery of small interfering RNA therapies.
In an Oct. 6 announcement, the company highlighted six proprietary preclinical programs spanning metabolic, renal, respiratory and central nervous system diseases. More than half have completed animal efficacy testing, according to XtalPi. For pharmaceutical R&D teams, the potential benefit is a connected workflow in which experimental results inform the next round of AI-generated designs.
siRNA drugs work by silencing disease-driving genes before they produce proteins, potentially opening paths to targets that are difficult to address with conventional drugs. But designing effective sequences, selecting chemical modifications, proving activity in animals and delivering the molecules outside the liver remain major development challenges.
How Kodexia works
At the center of Kodexia is XtalPi’s proprietary siFormer architecture, which combines RNA interference biology with nucleic acid chemistry. The system uses factors such as RNA thermodynamics, strand loading, target accessibility and silencing efficiency when generating candidate molecules.
That matters because siRNA discovery is not simply a matter of finding a sequence that works in a laboratory test. A promising design must also survive the jump into an animal, maintain activity, avoid unwanted effects and potentially clear intellectual property hurdles.