Phase 2 Ovarian Cancer Trial, Recruiting NCT07024784 Sponsor: AbbVie Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07024784
Recruiting Phase 2

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:

  • You are in generally good health and able to carry out daily activities with little or no limitation (this is measured on a standard scale called ECOG, scoring 0 or 1)
  • You have been diagnosed with a specific type of ovarian, fallopian tube, or peritoneal cancer called high-grade serous epithelial cancer
  • In most cases, your cancer must have at least one tumor that can be clearly measured on a scan
  • Any previous cancer treatment (such as chemotherapy) must have finished at least 4 weeks ago (or sooner, depending on the specific drug used)
  • If you received targeted radiation therapy, it must have been completed at least 2 weeks before starting this trial

Who may not be able to join:

  • You have a type of ovarian cancer classified as endometrioid, clear cell, mucinous, sarcomatous, mixed, low-grade, or borderline (confirm with trial site)
  • You have a significant medical condition or other health issue that the trial doctor believes could interfere with your participation or make the treatment unsafe for you
  • You have previously received a treatment that targets a protein called FRα (folate receptor alpha) (confirm with trial site)
  • You have previously had large-area radiation therapy that affected more than 20% of your bone marrow

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 15 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: ABBVIE INC., AbbVie

Phone: 844-663-3742

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
Registry
ClinicalTrials.gov
Start date
30 July 2025
Est. completion
1 January 2028

Where this trial is recruiting

🇮🇱 Israel 🇯🇵 Japan 🇺🇸 United States

Primary endpoints

Number of Participants With Dose-limiting Toxicities (DLTs); Percentage of Participants with Adverse Events (AE)

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: 15 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