Myelodysplastic Syndromes (MDS)

Position Your MDS Drug Asset Across the AML Transition Window

Built on ImpriMed’s myeloid expertise, xCellSense® applies ex vivo drug-sensitivity and synergy testing to high-risk MDS and the MDS-to-AML transition.

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OTHER INDICATIONS
AMLALLNHLMMMDS

The MDS development challenge

High-risk MDS shares biology with AML and frequently progresses to AML. Venetoclax/HMA combinations and novel agents require functional positioning, and AML-transition risk shapes both patient selection and endpoint strategy.

What we test in MDS

1

Functional positioning
Sponsor asset ±venetoclax, HMA, and standard of care in live-derived primary MDS cells, with synergy quantification

2

Activity benchmarking
vs. standard of care in high-risk samples

3

Myeloid biomarker correlation
Genotype-to-response association using our AML methodology

4

Transition-relevant insight
Profiling oriented toward the high-risk MDS/AML-transition setting

Platform applicability

MDS is supported by our extensive myeloid (AML) ex vivo program, which shares methodology, panel, and biology with high-risk MDS — applied to your MDS questions in a custom-designed study.

Why it de-risks development

Functional positioning versus standard of care, AML-transition-relevant insight, and enrichment hypotheses for MDS trials.

Key Deliverables

01
Ex vivo drug sensitivity + synergy on primary high-risk MDS cells
02
VEN/HMA benchmarking vs. standard of care
03
Myeloidgenotype-response correlation
04
Responder segmentation and enrichment hypotheses
05
Interpretation and dataset with a fast turnaround time
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Scope a MDS Study

A scientist — not a sales desk — will scope a tailored MDS study and return a design and timeline.