Tests living tumor cells to observe actual cell death, growth arrest, and resistance, rather than inferring response from genetics alone.
Interrogates single agents and rational combinations to surface potential synergy or antagonism for an individual patient.
Ranks therapies by observed effect and presents results as an interpretable SynRx™ Response Profile for clinician decision‑making.
Supports re‑testing when the disease evolves, aligning therapy with the tumor’s changing behavior.
SynRx™ integrates cell biology, quantitative cytometry, and analytics to create a patient‑specific functional fingerprint.
No. Genetic and molecular tests identify mutations that may hint at sensitivity or resistance. SynRx™ observes functional response directly, how living tumor cells react to therapies, so the methods are complementary.
Testing requires a fresh, viable specimen with adequate cellularity. Yield and tumor heterogeneity may affect feasibility or scope.
Panels reflect clinical context and practicality. Not every agent can be tested, and clinical judgment remains essential.
No. SynRx™ is a decision‑support tool. Results are interpreted by clinicians within each patient’s broader medical picture.