Advancing Cancer Care and expanding the boundaries of Personalized Medicine


Current applications address critical unmet needs in cancer care.
Future direction includes expanded therapeutic areas.

Addressing Critical Unmet Needs and Costly Trial-And-Error Approaches

Tumor Cell Testing

Why: Less than 25% of late-stage cancer
patients benefit from current approaches
- Direct measurement of drug response
- 48-hour rapid turnaround time
- Broad validations for true personalization
- CLIA-certified laboratory
- Enhanced therapy selection
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Immunotherapy Response Prediction

Why: Limited biomarker effectiveness
and high treatment failure rates
- Blood-based testing
- Multiparametric analysis
- Complementary to existing biomarkers
- Expand treatment options to recover response
- Comprehensive immune assessment
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Current Travera Solutions

01
3-4x Improved Therapy Selection
Travera's innovative biophysical platform accurately measures how cancer cells respond to therapies, delivering a 3-4x improvement in response prediction and informing expanded therapeutic options
02
Universal Application
Our technology works across virtually all cancer types and treatment modalities including cytotoxics, targeted inhibitors, and immunotherapies, eliminating the limitations of traditional biomarker approaches. Travera's platform has been validated in solid tumors and hematologic malignancies, demonstrating consistent performance regardless of cancer origin.​
03
Rapid and Cost-effective Approach
Results delivered within days, not weeks, enabling faster clinical decision-making when time matters most. Our streamlined workflow eliminates complicated processing steps and expensive sequencing, providing actionable insights at a fraction of the cost of comprehensive genomic profiling.
Market Reaction
“As our patients use the Travera test, the Cancer Commons database will show which drugs and cancer subtypes get the most accurate therapy guidance.”
Marty Tenenbaum
Founder, Cancer Commons

Clinical Evidence

Travera's comprehensive clinical validation program confirms the accuracy, reliability, and clinical utility of this single-cell biophysical platform.

By directly measuring how cancer or immune cells respond to therapies, providing actionable insights that translate to meaningful improvements in patient outcomes. This evidence-based approach ensures physicians can confidently integrate this technology into their clinical decision-making process.

Links:
2024 JCO Precision Oncology
2022 Nature Communications Biology
Multiple peer-reviewed publications
1000+ clinical samples and ongoing clinical trials
Real-world evidence

Link: AACR 2025

Development Pipeline

Novel Biomarker Development
Developing proprietary biophysical signatures for precision therapy selection

Advancing cell mass + multiparametric biomarkers for tumor and immune characterization​

Pioneering combination biomarker approaches that complement and enhance "–omics" based testing​

Expanding validation across additional cancer subtypes, rare tumors, and immune targets​

Creating standardized protocols for streamlined implementation in clinical settings​
AI/ML
Integration
Leveraging machine learning to enhance predictive accuracy of cellular response data

Developing algorithms to identify complex patterns in biophysical measurements

Creating integrated platforms that combine genomic and biophysical measurements to learn at a 20x scale​

Building predictive models that improve with additional patient data

Establishing AI-enabled decision support tools for clinical implementation
Expanded
Therapeutic Areas
Extending platform application beyond oncology to autoimmune conditions

Developing assays for neurological disease therapeutic response prediction

Exploring applications in regenerative medicine and cell therapy assessment

Advancing capabilities for rare disease therapeutic evaluation

Creating specialized protocols for pediatric applications and precision dosing