Precision starts here.
CureNavi gives cancer patients access to genomic testing and clinical trials wherever they live.
One platform, two clear benefits.
CureNavi connects patients and their treating physician with the specialists of leading academic cancer centers so that every patient gets access to the genomic tests and clinical trials their case calls for. We use AI to turn your medical history into a clear picture the specialists can act on.
For patients and families
- Access to genomic testing if relevant to your diagnosis.
- A clear view of the clinical trials that may be open to you.
- Free to use. Funded by research partners, never by you.
For office-based physicians
- Decision support aligned with the latest guidelines and active trial protocols.
- Less time spent compiling files, more time with your patient.
- A direct line to the specialists at our partner cancer centers.
Three steps. One clear recommendation.
You share your files and your doctor's contact details
You create an account, upload your medical documents and give us the contact of the treating physician who should receive our recommendations. You stay in control of your data at every step.
CureNavi structures your data and matches it against current options
Our system reads your file, structures it to medical data standards and checks against current guidelines and active clinical trials whether genomic testing is recommended and which trials may be a fit.
A specialist reviews and sends a clear recommendation
A specialist from our partner cancer center validates the analysis and shares an actionable recommendation with you and your doctor. If a trial is a fit, we put you in touch with the trial center only with your explicit consent.
Clinical authority, by design.
- Built as a spin-off of Charité Berlin.
- Every recommendation is explainable, traceable and physician-validated.
- GDPR-compliant by design. All data processing stays in the EU.
Charité
Spin-off
A spin-off of Charité Berlin, in partnership with its Department of Urology.
Launching with prostate cancer, scaling from there.
We are launching our first version for prostate cancer at Charité's Department of Urology, with a focus on access to genomic testing and clinical trial matching. Over the following months we will extend to further urological and molecularly driven cancer entities, and we will add personalised treatment recommendations as a next step.
Pick the path that fits you.
Whether you are a patient looking for access to a trial or genomic testing, or a physician interested in joining the network, we'd love to hear from you.
Our mission.
CureNavi makes precision oncology accessible by connecting patients, their treating physicians, and leading cancer specialists on a single, trusted platform. We do this without charging patients or hospitals: the service is funded by the value of the anonymised real-world evidence we generate.
The team.
Gaëlle Waltinger
Formerly VP Europe at Bausch+Lomb, prior experience at Novartis. INSEAD & ESCP graduate.
Prof. Dr. Thorsten Schlomm
Director of the Urology Clinic at Charité Berlin and founder of DNA-Med.
Jonathan Jeutner
Physician specialising in Urology at Charité, founder of My Tuko. LL.B. and B.Sc. from LSE.
Dr. Nadine Biernath
Physician at the Urology Clinic of Charité Berlin, specialist in clinical genetics.
Frequently asked questions.
What can CureNavi help me with today?
Today CureNavi focuses on two things: checking whether genomic testing is recommended for your case, and matching you with clinical trials that may be open to you. Personalised treatment recommendations will follow in a later release.
Is CureNavi free for me?
Yes. There are no costs for patients or for treating physicians. Our work is funded by research partners who license access to anonymised real-world data, never by you.
Do I need a referral from my doctor?
No, but CureNavi works in partnership with your treating physician. They need to confirm you are their patient, and they receive the final recommendation alongside you.
My doctor isn't in the network yet. Can I still join?
Yes. You can give us their details and we will reach out to invite them. We cannot guarantee they will join, but most physicians who hear about us do.
What if no clinical trial is a fit for me today?
Even if no trial fits today, we keep your case in our network. As new trials open, we re-check your file and alert your doctor if something relevant becomes available.
Get in touch.
We read every message. Tell us briefly who you are and how we can help. We will get back to you within a few working days.
For patients and families
If you would like access to genomic testing or a clinical trial through CureNavi, please reach out. We will guide you through the next steps.
For physicians
If you are an office-based urologist or oncologist and would like to join the network, write to us. We will set up a short call.
CureNavi GmbH
Berlin, Germany
info@curenavi.com