https://www.epo.org/en/news-events/in-focus/medical-technologies/personalised-medicine

Future of medicine: Personalised medicine

Last updated: 5.11.2025

Decorative image

For a growing number of patients today, visits to the doctor revolve around individualised genomic data, such as DNA markers linked to specific diseases and the efficacy of certain drugs.

Based on this patient-specific DNA data, healthcare providers can make informed choices about prescribing medications that work better for patients with specific DNA profiles, while avoiding medications established as less effective or dangerous. Doctors can also leverage DNA data to schedule specific preventative screenings and initiate targeted, genetic therapies.

Meet the inventors behind these pioneering technologies.


Carol Vivien Robinson

Advancing biochemistry with mass spectrometry

Dame Carol Robinson developed 'native mass spectrometry' to allow researchers to better understand proteins within their natural environments, paving the way for advancements in drug discovery and personalised medicine.

Read more


​​Landegren and Fredriksson are prolific inventors named in dozens of patents​

Sensitive and specific protein detection assays​

The Proximity Extension Assay (PEA), developed by Ulf Landegren and Simon Fredriksson, enables highly sensitive protein detection within cells by linking proteins to DNA strands, thereby producing measurable data. With applications ranging from early disease detection to personalised treatment planning, PEA holds significant promise for improving patient outcomes across diverse areas of medicine.

Read more


Gordana Vunjak-Novakovic

Advances in tissue engineering

Gordana Vunjak-Novakovic developed a new way of growing new tissue ex vivo (outside the body) using the patient's own cells. Her approach offers a safer, more precise and less intrusive facial reconstruction method and holds promise for replacing damaged lung and heart tissue.

Read more


Matthias Mann

Screening proteins to expose early signs of illness

Matthias Mann pioneered a method to identify, count and label every single protein in a tissue sample or bodily fluid such as blood. This in-depth analysis can reveal tell-tale signs of medical conditions before patients fall ill.

Read more


Jérôme Galon

A clearer cancer test

The technique developed by Jérôme Galon makes it possible to predict the risk of relapse for cancer patients. His test has improved the accuracy of cancer prognosis and helped tailor therapies to individual patients.

Read more


Jacek Jemielity, Joanna Kowalska, Edward Darżynkiewicz

A new approach to treating cancers and genetic defects

A research team lead by Jacek Jemielity, Joanna Kowalska and Edward Darżynkiewicz paved the way for personalised therapies with their method for stabilising mRNA. Their inventions are already used in several vaccines and anti-cancer medications.

Read more


Hans Clevers

Lab-grown human organs

Geneticist Hans Clevers and his team grew "mini-organs" - including livers, lungs and intestines - from stem cells of individual patients. This breakthrough allows doctors to safely test specific drug effects on an organ outside the body.

Read more


Laura van't Veer

Gene-based breast cancer test

The gene-based breast cancer test developed by Laura van ‘t Veer and her team determines the risk of cancer recurrence, identifying high-risk patients who require chemotherapy while sparing low-risk patients from the harsh side-effects of the treatment.

Read more


Cary L. Queen

The future of drug development

Cary L. Queen and Harold Edwin Selick invented humanised antibodies that contain at least 90% human components. Resulting treatments cause fewer adverse immune reactions, making them more effective against cancer and other diseases.

Read more


Christofer Toumazou

Microchip for quick DNA testing

Thanks to Christofer Toumazou's USB stick that decodes a patient's DNA within minutes, it is possible to identify genetic mutations that determine a person's predispositions to certain hereditary diseases.

Read more


Thomas Tuschl

Gene-silencing technique to treat diseases

Thomas Tuschl developed a method of "switching off" human genes. His gene silencing technique helps diagnose and treat a wide variety of conditions from haemophilia to high cholesterol.

Read more


Pål Nyrén

Fast efficient DNA sequencing

Pål Nyrén furthered genetic research and made it more efficient and affordable. His patented DNA sequencing method, known as Pyrosequencing, is one of the most common used today.

Read more


Jason Chin

Re-engineering protein synthesis

Custom-made proteins synthesised according to the method developed by Jason Chin and Oliver Rackham are revolutionising therapeutics. It is can also be used to detect prostate, ovarian, and colon cancer.

Read more


Christine Van Broeckhoven

Understanding and combating Alzheimer's

The work of Christine Van Broeckhoven has provided insight into why Alzheimer's develops in some individuals, shaped R&D in the field, and has helped develop new treatments for neurodegenerative brain diseases.

Read more


Jürg Zimmermann

New treatment, new hope

Patients with chronic myelogenous leukaemia (CML) were faced with painful treatments and no certainty of remission. This changed when Brian Druker and Jürg Zimmermann invented a treatment that zeroes in on a genetic abnormality found in 95% of patients with CML.

Read more


Karlheinz Schmidt

A replacement for organ transplants?

Inventor Karlheinz Schmidt devised an alternative to transplanting donor organs, growing body parts by using living stem cells as engineering materials. His "tissue engineering" method opens the door to organ replacements based on the patient's individual DNA profile.

Read more


Wojciech Stec

Workhorses of Molecular Biology

The building blocks for new, targeted therapies - namely DNA and RNA components - can be produced cost-efficiently and on an industrial scale thanks to the invention by Polish researcher Wojciech Stec.

Read more