Information for patients and families

A cancer diagnosis can feel overwhelming. Navignostics is developing advanced molecular analysis to give oncologists a more detailed picture of individual tumors, with the goal of supporting better-informed treatment decisions.

This page explains what we do, who can currently access our analysis, and how to find out whether it may be relevant to your situation.

Where we are in our development: Our analysis is currently classified as Research Use Only (RUO) and are not yet approved as a clinical diagnostic test by regulatory authorities. Access to our analysis is currently available within specific research programs at partner institutions in Switzerland and Europe. We are working towards full regulatory approval. If you are unsure whether this is relevant to your situation, please speak with your oncologist.

Why standard testing isn't always enough

Every cancer is different. Even two patients with the same diagnosis can have tumors that behave very differently.

Standard pathology tells your doctor a lot, but it may not fully capture how your tumor is organized at a molecular level: which proteins and drug targets are present, how immune cells are interacting with tumor cells, and what could stop a treatment from being successful.

Think of it this way: standard tests can tell you which street names are in a town. Our analysis plots those streets on a map, showing how they intersect, whether they’re one-way, and where the dead-ends are. That level of detail can matter when your oncologist is deciding which treatment path to take.

What Navignostics does

Immune
Tumor
,

Slide the arrows to reveal the immune and tumor cells of a melanoma tumor.

Navignostics is developing a diagnostic test that analyses your tumor using a technique called spatial single-cell proteomics.

In simple terms, we look at lots of different proteins at the same time inside your tumor. This includes cancer cells, immune cells, and the tissue surrounding them. We then create a map of your tumor that is far more detailed than what standard tests can provide.

The results are compiled into a report for your oncologist or pathologist. Navignostics does not prescribe treatments or make clinical decisions, all treatment decisions remain entirely with your treating oncologist.

How we process your sample

1. Your oncologist sends us a small part of your already-taken biopsy sample to our central laboratory in Switzerland. No additional clinical procedures are necessary.

2. We measure and analyze your sample with our technology, creating a detailed map of all the immune and tumor cells and how they interact.

3. Your report is sent to your oncologist, who will discuss the findings with you in the context of your overall care. How findings inform your treatment is always determined by your oncologist.

Can I access the Navignostics analysis now?

In some cases, yes. 

Navignostics analysis is not yet available as a standard test your doctor can simply order. However, if you have a solid tumor cancer, there may be a pathway to access our analysis within a research context with one of our research partners.

We are currently most active in late-stage research contexts in the following indications: lung cancer, colorectal cancer, melanoma and breast cancer.

The best starting point is to ask your oncologist whether they would be interested in collaborating with the doctors at our partner institutions to receive a Navignostics analysis. 

You can ask them to reach out to us directly for more information.

What your results may show

A close up of a slide

Potential therapy options

The report may show molecular features relevant to targeted or immunotherapy approaches for your oncologist to weigh alongside other clinical information.

Less effective therapies

With the same information, oncologists may see features that suggest certain treatments may be less appropriate, helping to focus discussion on the most relevant options.

Clinical trial relevance

Your oncologist may see molecular characteristics that are relevant to clinical trials they will consider discussing with you.

These findings are provided to support your oncologist’s analysis, they are not a clinical recommendation on their own. Your doctor will interpret them in the context of your full clinical picture.

Frequently asked questions

Can I request this analysis myself?

Not directly. The analysis is initiated by your treating oncologist within the context of a research program. If you think it could be relevant to your care, the best step is to raise it with your oncologist. You are also welcome to contact us and we can provide information that you can share with your oncologist.

Not yet. Our platform is currently classified as Research Use Only (RUO) and is not approved as a clinical diagnostic. We are conducting the studies needed to support our CE-IVD regulatory submissions. Your oncologist can advise on what this means in practice for your situation.

In most cases, no. Our analysis is performed on tumour tissue from a biopsy or surgical specimen that has already been collected. Your pathology team will assess whether the available material is sufficient.

We aim to do the analysis as quickly as possible. Turnaround time depends on the specific analysis and current capacity. Your oncologist can ask for an estimated timeframe when contacting us.

Our analyses are currently conducted within research programs and are not reimbursed through health insurance. Costs are typically covered by research funding. Your oncology team can confirm what applies in your situation.

Your data is handled in accordance with Swiss and EU data protection law, including the revised Swiss Federal Act on Data Protection (revFADP) and, where applicable, the GDPR. Tissue handling follows standard clinical and ethical requirements. Any use of patient material beyond the requested analysis requires appropriate consent.

This can happen. Not every tumor produces a definitive molecular signal. When findings are uncertain, the report will reflect that clearly, and your physician will use it as one input alongside all other available information. An inconclusive result does not mean the analysis has failed, it means the molecular picture is complex, which is itself useful clinical context.

Reports are sent directly to your treating oncologist. You can request a copy through your clinical team.

We are a start-up and not yet well known in all clinical settings. If you would like your oncologist to learn more, you can ask them to contact us directly. We are happy to provide scientific and clinical information to support the conversation.

We are not in a position to confirm timelines. Regulatory approval depends on the completion of analytical performance studies and the assessment of the relevant authorities. We are actively working towards this and will communicate progress here and through our other channels.

Disclaimer: The information on this page is for general informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional regarding your medical condition and treatment options. Navignostics does not make clinical recommendations directly to patients.

Regulatory status: Navignostics analytical methods are classified as Research Use Only (RUO) and are not approved diagnostic devices. They are not intended to be used as the sole basis for clinical decisions. This applies in all jurisdictions including Switzerland, the EU, and the United States.