Phase 4 Ovarian Cancer Trial, Not Yet Recruiting NCT06887933 Sponsor: GlaxoSmithKline Condition: Ovarian Cancer
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Phase 4 Ovarian Cancer Trial, Not Yet Recruiting

NCT06887933
Not Yet Recruiting Phase 4

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who may be able to join

  • Women aged 18 or older who are able to understand the study procedures and agree to take part by signing a written consent form.
  • People who have been diagnosed with epithelial ovarian cancer confirmed through laboratory tissue testing.
  • People whose cancer meets the approved treatment criteria as a maintenance therapy for advanced (Stage III or IV) high-grade ovarian, fallopian tube, or primary peritoneal cancer, where the cancer has responded (fully or partially) after completing a first course of platinum-based chemotherapy.
  • People whose cancer meets the approved treatment criteria as a maintenance therapy for platinum-sensitive relapsed high-grade ovarian, fallopian tube, or primary peritoneal cancer, where the cancer has responded (fully or partially) to platinum-based chemotherapy.
  • People whose blood test results meet the required levels: a certain type of white blood cell count (neutrophils) of at least 1,500 per microlitre, platelets of at least 100,000 per microlitre, and haemoglobin of at least 9 grams per decilitre (confirm with trial site).
  • People whose high blood pressure is adequately controlled, as assessed by the treating doctor.
  • Women who are able to become pregnant must be willing to use contraception throughout the study and for 180 days after the last dose of the study treatment.

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People who are pregnant, breastfeeding, or planning to become pregnant during the study or within 180 days after the last dose of study treatment.
  • People with known active liver disease, end-stage kidney disease, a serious uncontrolled medical condition, or a known history or current diagnosis of certain blood-related conditions (Myelodysplastic Syndrome or Acute Myeloid Leukaemia).
  • People who have previously received a type of cancer treatment known as a PARP inhibitor.
  • People with a serious uncontrolled medical illness occurring at the same time as the study.
  • People who would be receiving the study drug in a way that does not match its approved use.
  • People with a known history of allergic reaction to the study drug, its ingredients, or medications from a similar drug class.
  • People who have previously or currently been diagnosed with Myelodysplastic Syndrome, Acute Myeloid Leukaemia, or an inflammatory lung condition called pneumonitis.
  • People who have not sufficiently recovered from a previous surgery or cancer treatment.
  • People with a known history of Hepatitis B or Hepatitis C.
  • People with an active infection such as tuberculosis (TB).
  • People who have taken part in another clinical study involving a study drug within the last 3 months.
  • People who, in the treating doctor's judgement, are unlikely to follow the study procedures, rules, and requirements.
  • People who have previously been enrolled in this same study.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 9 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Phone: 877-379-3718

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Not Yet Recruiting
Phase
Phase 4
Sponsor
Registry
ClinicalTrials.gov
Start date
22 April 2025
Est. completion
20 March 2026

This date has passed while the registry still lists the trial as open to participants. Sponsors often update a trial's status without revising its projected end date, so it may well still be recruiting — but the record is out of date in at least one respect. Check with the study contact before relying on either.

Primary endpoints

Number of participants with treatment-emergent adverse events (TEAEs)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov