Phase 2 Ovarian Cancer Trial, Recruiting NCT06682988 Sponsor: AbbVie Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT06682988
Recruiting Phase 2 🇦🇺 Australian site

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

  • People who have been diagnosed with high-grade serous ovarian cancer, primary peritoneal cancer, or fallopian tube cancer (confirmed by testing).
  • People whose cancer has stopped responding to platinum-based chemotherapy in one of these ways: those who had 1 previous course of platinum-based treatment (at least 4 cycles), showed some response, but then had cancer growth between 3 and 6 months after their last platinum dose; OR those who had 2 or 3 previous courses of platinum-based treatment and had cancer growth within 6 months of their last platinum dose.
  • People whose cancer has been confirmed by imaging to have grown or spread during or after their most recent treatment.
  • People who are in good enough general health to be rated 0 or 1 on the ECOG scale, meaning they are either fully active or have minor restrictions on physically demanding activity (confirm with trial site).
  • People who have at least one area of cancer that can be measured on a scan, according to standard measurement guidelines called RECIST v1.1.
  • People whose tumor tests positive for a protein called folate receptor alpha (FRα) at a specific level of expression, as measured by a particular laboratory test.

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 whose ovarian cancer is a specific type other than high-grade serous, including endometrioid, clear cell, mucinous, or sarcomatous types, mixed tumors containing any of those types, or low-grade or borderline ovarian tumors.
  • People whose cancer never responded to their very first platinum-based chemotherapy, or whose cancer grew within 3 months of their last dose of first-line platinum treatment.
  • People who have a serious concurrent illness or an active infection considered clinically significant, as defined in the trial protocol (confirm with trial site for specifics).
  • People who have had a stroke (either bleeding in the brain or a blocked blood vessel) within the 6 months before joining the trial.

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 31 July 2026

Contact this trial

Principal Investigator: ABBVIE INC., AbbVie

Phone: 844-663-3742

Australian sites

Blacktown Hospital /ID# 272182, Blacktown, New South Wales
Newcastle Private Hosptial /ID# 272213, Lambton Heights, New South Wales
Royal Brisbane and Women's Hospital /ID# 272123, Brisbane, Queensland
Icon Cancer Centre Chermside /ID# 272220, Chermside, Queensland
Ballarat Base Hospital /ID# 272240, Ballarat, Victoria
Monash Health - Monash Medical Centre - Clayton /ID# 272234, Clayton, Victoria
Sir Charles Gairdner Hospital /ID# 272116, Nedlands, Western Australia

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

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
28 May 2025
Est. completion
1 July 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.

Where this trial is recruiting

🇦🇺 Australia 🇧🇪 Belgium 🇫🇷 France 🇵🇱 Poland 🇰🇷 South Korea 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Randomized Phase 2 Cohort: Percentage of Participants with Grade >= 2 Treatment-Emergent Corneal Adverse Events (AEs); Randomized Phase 2 Cohort: Percentage of Participants who Achieved Objective response rate (ORR); Hepatic Impairment Cohort: Maximal Concentration (Cmax) of Mirvetuximab Soravtansine; Hepatic Impairment Cohort: Area Under the Plasma Concentration (AUC) of Mirvetuximab Soravtansine; Hepatic Impairment Cohort: Trough Concentration (Ctrough) of Mirvetuximab Soravtansine; Hepatic Impairment Cohort: Volume of Distribution at Steady State (Vss) of Mirvetuximab Soravtansine; Hepatic...

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: 31 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