A clinical trial investigates how well new or improved treatments work - for example, drugs, combinations of therapies or new diagnostic procedures. The aim is to further develop and improve treatment options for people with cancer.

Only through trials can we find out whether a new therapy actually works better than the previous one. Your participation will help to improve the cancer treatment of tomorrow - for you and for many other patients.

Yes, safety is our top priority.
Before a trials begins, it is carefully examined and approved by experts and the relevant authorities. During the trial, you will be closely supervised and medically monitored.

Your personal data and any samples you provide (e.g. blood or tissue) will be treated in strict confidence. They will only be used for scientific purposes and secured in accordance with the highest data protection standards.

No. Participation is voluntary.
You decide for yourself whether you want to take part - and you can end your participation at any time without giving reasons. This will not affect your regular medical care.

After a detailed discussion with the investigator, all details of the trial will be explained. You will receive a written declaration of consent, which you can read at your leisure. Only when you feel confident will you make your decision.

An experienced medical team is at your side - right from the start. You will be examined regularly, your questions will be taken seriously at all times and you will receive close support throughout the trial.

You may have access to new therapies - even before they are widely available. At the same time, you make an important contribution to research and to improving treatment for other cancer patients.