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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.
US: Kathleen Moore
+1 405-271-8707
KathleenMoore@ouhealth.com
Europe: Rebecca Kristeleit
Rebecca.Kristeleit@gstt.nhs.uk
Ovarian Cancer
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.
The patient's local archival tumor tissue (FFPE) from original tumor, or from the metastatic tissue, will be collected to potentially identify if they - at a later stage of their disease - will be likely to benefit from treatment with any of the investigational cancer drugs available to Allarity Therapeutics. Data from this study can further be used to explore in a retrospective fashion, sensitivity to other chemotherapeutic drugs previously used in the treatment of their ovarian cancer, to investigate whether or not the DRP® method can predict and confirm the obtained sensitivity to the prior given drugs as well as prospective analyses guiding the Investigators on future treatments.
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.
US: Kathleen Moore
+1 405-271-8707
KathleenMoore@ouhealth.com
Europe: Rebecca Kristeleit
Rebecca.Kristeleit@gstt.nhs.uk
The study is sponsored by Allarity Therapeutics and is in collaboration with Amarex Clinical Research.
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.
