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Clinical Pre-screening Protocol for Ovarian Cancer

Sponsor: Allarity Therapeutics

NCT ID: NCT03877796

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Drug Response Predictor® (DRP) (device)
How long the study runs
Study runs about 104 months (dates as stated)
About the drug or intervention
Drug Response Predictor® (DRP) — device: A DRP is an assay that based on samples from a tumor can predict whether the tumor will respond to a specific drug or not.
Patient visit burden
Not specified by the sponsor

In plain English

This is a screening list for a clinical trial looking at ovarian cancer, run by a company called Allarity Therapeutics. It is for people with a type of ovarian cancer called epithelial ovarian cancer that has come back or got worse despite treatment. The trial team uses this list to see who might be able to join.

Who can take part

  • You have epithelial ovarian cancer confirmed by looking at tissue under a microscope.
  • Your cancer got worse within 6 months of finishing platinum-based chemotherapy, or you cannot have platinum treatment for another reason.
  • You have had no more than one previous course of treatment after your cancer stopped responding to platinum chemotherapy (or if you could not have platinum at all).
  • A sample of your tumour tissue, stored in wax (called FFPE tissue), is available for testing.

Who may not be able to

  • Your cancer got worse while you were still having platinum-based chemotherapy (doctors call this platinum-refractory disease).
  • You have had another type of cancer, unless it was stage I or II and the study doctor believes it has been cured.

What taking part involves

  • • Not stated — ask the trial team

Time commitment: Not stated — ask the trial team about visits, how long the trial lasts, and what taking part would involve.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
18 Years and over
Who
Female
Number of participants
60
Started
2019-04-11
Last checked
2026-07

Plain English Summary

What is this study?

  • • Testing a new treatment for ovarian cancer
  • • Clinical study - 60 participants
  • • 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

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with ovarian cancer
  • • Female only

Where?

  • • Glasgow - Beatson West of Scotland Cancer Centre
  • • London - Guy's and St Thomas' NHS Foundation Trust, Guy's Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

Ovarian Cancer

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: Female only

Treatment history

Treatments you must have had:

  • ✓ of therapy in the platinum resistant

What the study is looking for

  • ✓Patients with histological confirmed epithelia ovarian cancer
  • ✓Patients must have platinum-resistant disease, defined as progression within 6 months after the last dose of...
  • ✓Patients have received no more than one previous treatments in the platinum resistant or platinum ineligible setting
  • ✓FFPE tumor tissue available

Who cannot take part

  • ✗Patients who have platinum-refractory disease, defined as progression during the last platinum-based drug treatment.
  • ✗Other cancer with exception of any stage I and II cancer that is deemed cured by the Investigator
See the full 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 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

Where Is This Study? (2 UK sites)

Beatson West of Scotland Cancer Centre

Glasgow G12 0YN, United Kingdom

Recruiting
Site contact (verified)
Ros Glasspool, MDPrincipal Investigator

Guy's and St Thomas' NHS Foundation Trust, Guy's Hospital

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Main Email: gstt.research.rbhh@nhs.net

gstt.research.rbhh@nhs.netn/a

How to Get in Touch

US: Kathleen Moore

Sponsor contact

CONTACT

+1 405-271-8707 KathleenMoore@ouhealth.com

Europe: Rebecca Kristeleit

Sponsor contact

CONTACT

Rebecca.Kristeleit@gstt.nhs.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-07