Eliminate costly drug development failures –– leverage real human biology for confident decisions

ImpriMed has developed a proprietary method for analyzing ex vivo drug sensitivities (DS) of anticancer drugs,
enabling direct measurement of therapeutic effects on live patient cancer cells.
Traditional preclinical models fail to capture the complexity and heterogeneity of real human disease — limiting their ability to predict clinical response.
ImpriMed provides human-relevant ex vivo testing on live patient samples, offering early, data-driven insight into clinical performance.
Biologics with direct cytotoxic effects
Small molecules
Peptides
Oligonucleotides
Enzymes

Drug sensitivity testing

Combination synergy analysis

Advanced analytics using AI

Specialized in hematologic malignancy
xCellSense™ Functional Testing identifies patients most likely to respond, enables smarter enrollement strategies, and supports trial enrichment and precision-driven design.
AI-powered Risk Stratification for:
ImpriMed's Proprietary Optimum Media maintains high ex vivo viability and stability of blood cancer patients' primary cells after biopsy







1
Human‑Relevant Biology
We test compounds directly on primary patientsamples, capturing the true heterogeneityof hematologic malignancies.
2
Faster, Lower‑Risk Development
Generate clinically meaningful insights in weeks 〞not months, reducing uncertaintybefore entering the clinic.
3
Better Trial Design & Patient Selection
Identify responsive patient subgroups through:
4
Differentiation in a Competitive Landscape
Strengthen IND packages, investor materials,and partnership discussionswith real-world functional data.
We help clients:

ImpriMed provides a human-relevant, predictive, and scalable ex vivo CRO service designedto accelerate development, sharpen clinical strategy, and improve the probability of clinical success.

ImpriMed began receiving pancreatic cancer samples in November 2025, and both indications are currently being integrated into our service portfolio.
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