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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Anthony Kong
44+2078486004
Anthony.Kong@kcl.ac.uk
Ifigenia Vasiliadou
44+2078486004
Ifigenia.1.Vasiliadou@kcl.ac.uk
Squamous Cell Carcinoma of Head and Neck
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
This study aims to investigate the efficacy and safety profile of superficial hyperthermia (wIRA) in addition to standard of care (SOC) palliative radiotherapy in patients with inoperable/incurable locally advanced or recurrent/metastatic HNSCC or cutaneous SCC superficial tumours not suitable for radical treatment.
The investigators will assess the best objective response rate (ORR) of patients with Inoperable/incurable or recurrent/metastatic HNSCC or cSCC with superficial lesion(s) treated with the combination of superficial hyperthermia (wIRA) and palliative radiotherapy.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
You can take part if:
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Ifigenia Vasiliadou
44+2078486004
Ifigenia.1.Vasiliadou@kcl.ac.uk
Anthony Kong
44+2078486004
Anthony.Kong@kcl.ac.uk
The study is sponsored by King's College London and is in collaboration with Guy's and St Thomas' NHS Foundation Trust.
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
