Clinical Pre-screening Protocol for Ovarian Cancer
Recruiting
Observational Study
Ovarian Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Female
Study type
Observational
Participants needed
60 (estimated)
Sponsor
Allarity Therapeutics · Industry
Who this trial is looking for
This trial is looking for patients with ovarian cancer to see if their tumor tissue can help identify effective treatments. Participants will provide tissue samples to help understand how they might respond to different cancer drugs.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with epithelial ovarian cancer
I have platinum-resistant disease, meaning my cancer has progressed within 6 months after platinum chemotherapy, or I cannot receive platinum-based treatment
I have received no more than one previous treatment for my platinum-resistant or platinum-ineligible condition
I have tumor tissue available for testing
You may not be able to join if
I have platinum-refractory disease, meaning my cancer progressed during platinum chemotherapy
I have another cancer, except for stage I or II cancers that my doctor says are cured
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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, sensitivi…
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with histological confirmed epithelia ovarian cancer
* Patients must have platinum-resistant disease, defined as progression within 6 months after the last dose of platinum-based chemotherapy, or are platinum ineligible.
* Patients have received no more than one prior…
Inclusion Criteria:
* Patients with histological confirmed epithelia ovarian cancer
* Patients must have platinum-resistant disease, defined as progression within 6 months after the last dose of platinum-based chemotherapy, or are platinum ineligible.
* Patients have received no more than one prior line of therapy in the platinum resistant or platinum ineligible setting
* FFPE tumor tissue available
Exclusion Criteria:
* Patients who have platinum-refractory disease, defined as progression during the last platinum-based chemotherapy.
* Other malignancy with exception of any stage I and II cancer that is deemed cured by the Investigator
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