Detecting what matters

Accurate patient stratification remains one of the most pressing challenges in ADC development. At Bavarian Biotech, we’ve developed High-Affinity Probes (HAPs) that reveal whether ADCs can bind to their intended targets in real tumor tissues. Unlike IHC or genetic assays, HAPs mimic the therapeutic itself, making them the only tool that can directly assess drug-target engagement in fixed patient samples. This gives ADC developers and researchers unprecedented insight into binding-site accessibility, improving target validation, patient stratification, and translational research.

Key Features:

  • Direct Measurement of Target Accessibility: Unlike traditional methods, HAPs measure functional binding-site accessibility, offering a more accurate assessment of whether an ADC can effectively target its antigen.
  • Works with FFPE TissueHAPs are optimized for use with FFPE tumor samples, the standard tissue format in diagnostic and clinical settings, enabling seamless integration into existing workflows.
  • Flexible and Scalable: HAPs can be applied across all stages of drug development, from early preclinical studies to late-stage clinical trials, providing valuable insights into patient selection and biomarker validation.
  • Potential for Companion Diagnostics: HAPs can be converted into monoclonal antibodies (mAbs) that can be used as IVDR-certified assays, offering a potential pathway for companion diagnostic development in the future.
  • Enhances ADC StratificationBy providing functional insights into drug-target interactions, HAPs enable efficient patient stratification, helping to optimize clinical trial design and maximize ADC therapy success.

Same Target - Different Binding

Not all drugs that target the same protein will bind equally — or at all — in patient tissues. Despite being designed for the same molecular target, ADCs can show dramatically different binding profiles depending on their specific epitope, the tumor microenvironment, and structural accessibility. These differences are often invisible to conventional diagnostics like IHC, FISH, or sequencing. By mimicking therapeutic binding with high precision, HAPs provide a level of insight into drug-target engagement in tissue that is not accessible through conventional assays — offering a powerful tool for translational research and patient stratification.

Multiplexing: Visualizing Complexity in a Single Tissue Section

High-affinity probes (HAPs) can be multiplexed to simultaneously visualize multiple ADC targets within the same tumor section. This allows researchers to map spatial binding patterns, identify distinct tumor subpopulations, and uncover co-expression or exclusivity of therapeutic targets. By revealing how different ADCs bind across the tumor landscape, HAP multiplexing enables the generation of hypotheses around combination strategies, optimal treatment sequencing, and potential mechanisms of resistance.

Technology & Applications

High-Affinity Probe (HAP) technology provides a precise and versatile platform for detecting therapeutic binding sites on tumor tissues. Our probes are engineered for high specificity and sensitivity, enabling in situ quantification of binding site accessibility and density. 


HAPs integrate seamlessly into various workflows, from preclinical drug development to exploratory clinical research, supporting applications such as drug-target interaction mapping, patient stratification, and therapy exploration for challenging cases. The technology enhances precision in oncology research by delivering actionable molecular insights that drive innovation across the drug development pipeline.

Contact us

For more information or to get started, please reach out to us at info@bav.bio or use the contact form below. Our team will respond promptly to assist with your inquiry and provide the information you need. We look forward to hearing from you.