Phase 2 Ovarian Cancer Trial, Recruiting NCT07023627 Sponsor: Incyte Corporation Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07023627
Recruiting Phase 2 🇦🇺 Australian site

Who may 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 might be able to join this trial:

  • People who have been confirmed by tissue testing to have a specific type of cancer called high-grade serous cancer, affecting the ovaries, fallopian tubes, or the lining of the abdomen (peritoneum).
  • People whose cancer has stopped responding well to platinum-based chemotherapy — specifically, those who had only one course of platinum chemotherapy and received at least 4 cycles of it, or those who had two to four courses of platinum chemotherapy and whose cancer came back or worsened during or within 6 months of the last dose.
  • People who are willing to have a small tissue sample (biopsy) taken before treatment begins — a fresh sample is preferred, but a stored sample from within the last 5 years may be acceptable.
  • People who have received at least 1 but no more than 4 prior rounds of systemic (whole-body) cancer treatment since their diagnosis, and for whom a single cancer drug given on its own is considered a suitable next treatment option.
  • People who have previously been treated with a drug called bevacizumab, unless there was a medical reason preventing its use.
  • People whose tumour tests positive for a protein called FRα must have previously been treated with a drug called mirvetuximab soravtansine, unless a medical reason prevented its use.

Who may not be able to join:

  • People whose cancer is of a different tissue type, such as endometrioid, clear cell, mucinous, or sarcomatous, including mixed tumours containing any of these types, or those with low-grade or borderline ovarian cancer.
  • People whose cancer never responded to their very first course of platinum chemotherapy, or whose cancer came back or worsened during or within 3 months of finishing that first course.
  • People whose tumour tests positive for FRα but who have not received mirvetuximab soravtansine for any reason other than a medical contraindication.
  • People who have had a significant or uncontrolled heart condition within the 6 months before the first dose of the study drug.
  • People with known active cancer that has spread to the brain or spinal cord lining.
  • People who have another cancer that is currently growing or requires active treatment.

Note: Other eligibility criteria set out in the study protocol may also apply (confirm with trial site).

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 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Incyte Medical Monitor, Incyte Corporation

Phone: 1.855.463.3463

Australian sites

Blacktown Cancer & Haematology Centre-Blacktown Hospital, Blacktown, New South Wales
Concord General Repatriation Hospital, Concord, New South Wales
Burnside War Memorial Hospital - the Brian Fricker Oncology Centre, Adelaide, South Australia
Hobart Hospital-Royal Hobart Hospital, Hobart, Tasmania
Cancer Research Sa (Crsa), Adelaide,
Southern Oncology Clinical Research Unit, South Australia,

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
Recruiting
Phase
Phase 2
Sponsor
Incyte Corporation
Registry
ClinicalTrials.gov
Start date
12 November 2025
Est. completion
27 April 2027

Where this trial is recruiting

🇦🇺 Australia 🇧🇪 Belgium 🇯🇵 Japan Puerto Rico 🇪🇸 Spain 🇨🇭 Switzerland 🇬🇧 United Kingdom 🇺🇸 United States

6 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Objective Response by IRC

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