Modeled by Cypre™: Proprietary hydrogel patterning technology builds consistent, high throughput 3D tumor models with complex biology such as T cell infiltration through the tumor stroma.
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Key Capabilities:

Cypre’s patented 3D modeling platform—built on Symphony® and VersaGel®—enables physiologically complex tumor organoids that mimic the architecture and biology of the human tumor microenvironment (TME). By integrating stromal fibroblasts, ECM density, and immune components, our models capture key factors that drive therapeutic response in vivo. The result is a high-throughput, reproducible system that supports efficacy and MOA screening with the translational rigor required for IND-stage decision-making.
Our 3D tumor organoids incorporate stromal fibroblasts, ECM tuning, and immune compartments—including T cells, NK cells, macrophages, and B cells—capturing the cellular cross-talk and immune exclusion seen in real patient tumors. This level of physiological complexity is essential for modeling drug response and resistance mechanisms with translational relevance.
Validated across chemotherapy, targeted therapies, immunotherapies, ADCs, and T cell engagers, our models are designed to reflect diverse treatment scenarios. Whether you're screening a single agent or a combination regimen, Cypre enables actionable insights for both early discovery and IND-stage programs.
From high-content imaging to cytokine profiling and flow-based phenotyping, our platform supports standardized, multi-modal analytics—delivering reproducible data across models, timelines, and modalities. Turnaround times as fast as 30–45 days help accelerate decision-making without compromising data depth.
Boehringer Ingelheim partnered with Cypre to evaluate a panel of T cell engagers across diverse PDX-derived tumor models—each designed to simulate an immune-excluded tumor microenvironment. The objective: assess tumor killing, T cell infiltration, and immune activation markers with greater physiological relevance than standard in vitro systems.
Using our proprietary VersaGel® hydrogel and standardized analytics, Cypre delivered detailed efficacy and MOA insights—including CD3⁺/CD8⁺ infiltration and cytokine profiles—in under 45 days. These results helped refine Boehringer’s lead optimization strategy and supported critical go/no-go decisions.
Models Screened across multiple tumor types using the Cypre 3D PDX platform
High-content imaging, cytokines, and flow cytometry readouts delivered
Full reports returned within 6–9 weeks, supporting timely go/no-go decisions
Data used in ongoing preclinical planning and pipeline strategy


Cypre’s models go beyond traditional tumor organoids by integrating not just tumor cells but also stromal fibroblasts, extracellular matrix (ECM) architecture, and a full suite of human immune cells — including T cells, NK cells, macrophages, and B cells. This multi-compartment design more accurately recapitulates the human tumor microenvironment (TME), enabling faster, more predictive insights into therapeutic efficacy and mechanism of action (MOA).


Yes. Our standardized analytics — including tumor growth inhibition, immune infiltration, cytokine profiling, and flow cytometry-based phenotyping — are delivered in a format suitable for regulatory submissions. Many clients leverage our Full Report™ as part of their IND strategy and preclinical data packages.


We return efficacy-only data in as little as 30 days, and full efficacy + MOA data in 45 days, depending on the panel selected. Custom studies typically run 8–12 weeks, with monthly intake slots available. Timelines are finalized during scope-of-work (SOW) development.


Absolutely. You can choose from our pre-configured 5-, 30-, or 42-model panels, or build a custom panel based on tumor indication, genomic profile (e.g., KRAS, BRAF, EGFR), or immune phenotype. Our team can help you select the right models to match your discovery or preclinical goals.


Start by filling out our brief intake form, which outlines your tumor model interests, analytics preferences, and target timelines. From there, we’ll generate a tailored Scope of Work and lock in your study date. To begin, schedule a call or contact us directly at hello@cypre.com.
Partner with Cypre to co-develop translationally validated, IND-ready insights using our complete 3D tumor organoid platform. From immune profiling to custom panels, we’re built for collaboration.