Find the responders in your trial data.
Find the responders in your trial data.
Predictive proteomic signatures from baseline blood that identify responders before treatment — analysis-only, your data stays in-house.
What we do
Many therapies work — but only in a subset of patients. ibiomic identifies that subset before treatment.
We analyze baseline blood proteomics from your existing cohort and derive compact, interpretable signatures that predict who will respond — so you can enrich enrollment, strengthen the label, and explain non-responders.
We are analysis-only: your samples and data stay in-house. We deliver the signature, the out-of-sample validation, and the biology — you keep ownership.
Our method is indication-agnostic; recent focus areas include immuno-inflammatory disease and oncology.
How it works
You share de-identified baseline proteomics (Olink / SomaScan) + response outcomes from a completed or ongoing cohort. Your samples and data stay in-house.
We discover minimal, interpretable signatures that separate responders from non-responders — cross-validated out-of-sample, returned as several equivalent panels, each with its biological rationale.
You confirm on a deployable assay. Your lab or CRO measures the selected proteins with a targeted clinical assay (e.g. ELISA / MS); we re-fit the formula to that platform — so the result is not Olink-only, but deployable.
You get a responder score — a single interpretable index, ready for trial enrichment, companion-diagnostic strategy, or standard assays.
Why ibiomic is different
Robust — stable across cohorts and measurement platforms.
Low-dimensional — a handful of proteins, not hundreds.
Interpretable — grounded in biological system behavior, not black-box models.
Redundant by design — we return several equivalent minimal panels, so you have a fallback if a protein or assay is unavailable. Penalized regression (LASSO / elastic net) gives you one fragile signature; we give you options.
Deployable — we bridge discovery to a targeted clinical assay and re-fit the formula, so you are not left with a research-only Olink signature.
Evidence
In published work, the method blindly recovered the gold-standard heart-failure marker NT-proBNP as one component of a two-protein signature — and added a second, novel axis — directly from proteomic data. Evidence that it finds real biology, not noise.
Who we work with
Translational medicine, biomarker, and clinical development teams in pharma and biotech. Our method is indication-agnostic — we work wherever baseline blood proteomics and response data exist. Recent focus areas include immuno-inflammatory disease and oncology.
How to start
The first step is a no-cost feasibility call: we review your trial and response data and scope a focused, paid pilot to find responder vs non-responder signatures in your data. The validated signatures, minimal panels, and biological interpretation are delivered in the pilot.
contacts@ibiomic.com
Contact
Interested in collaboration, early access, or learning more about ibiomic?
You can email us directly, or submit a request via this form.