We profile cell-free RNA-protein complexes to provide real-time, systems-level insights into disease biology, target engagement, and cellular response from a simple blood draw.
Genomic testing detects DNA mutations, but the dynamic state of disease, target expression, and therapeutic response is driven by transcriptional regulation. We bridge this gap by profiling cell-free RNA-protein complexes non-invasively.
Liquid biopsies are limited to detecting static DNA mutations, missing real-time changes in gene expression and cellular state.
Determining target expression and drug response inside deep tissues (liver, heart, brain) currently requires dangerous, invasive tissue biopsies.
Multi-billion dollar programs (siRNA, mRNA, ASO) lack real-time, cell-level validation of target engagement and safety inside patients.
The workflow begins with a routine, minimally invasive blood draw. NeXendia’s high-sensitivity platform requires less than 150 µL of plasma.
This ultra-low volume allows seamless integration into clinical trial protocols and serial, longitudinal patient monitoring.
Naked cell-free RNA degrades rapidly in biofluids, introducing massive noise. We focus instead on capturing **cell-free RNA-protein complexes**.
By selectively capturing intact, protein-protected RNA cargo, we preserve the biological signal that others throw away.
Once captured, we map the enriched complexes across three critical biological domains, profiling the cellular state of target organs:
The sequenced profiles are processed through our proprietary machine learning deconvolution models.
By filtering out over 90% of background noise, our algorithms resolve complex RNA fragmentation footprints into precise, tissue-specific biological signals.
Deconvolution translates raw sequence databases into quantitative proof of target engagement and safety.
We validate the platform via high-value biopharma drug co-development, while building a proprietary diagnostic atlas for early disease detection.
A universal window into disease state, active drug engagement, and real-time patient response.
Direct, cell-level validation of target engagement and pathway activation, measured from plasma without tissue biopsies.
Real-time profiling of organ-specific cellular response and tissue toxicity signals, de-risking safety early in development.
Building a proprietary database of cell-free RNA-protein signatures to discover novel disease targets and validate early multi-organ diagnostic indicators.
We are actively engaging with pharma and biotech partners to deploy our liquid biopsy platform in preclinical and clinical trials.