Skip to main content

A Study of Ocular Toxicity Evaluation and Mitigation During Treatment With Mirvetuximab Soravtansine in Participants With Recurrent Ovarian Cancer With High Folate Receptor-Alpha Expression

Active, not recruiting · Phase 2 · NCT06365853

Conditions: Recurrent Ovarian Cancer, Folate Receptor-Alpha Positive

At a glance

Research payments reported, 2025
$320,889
U.S. investigators named
12
Sites paid
12
Planned or actual enrollment
108

About the trial

Sponsor
AbbVie
Tested
Mirvetuximab Soravtansine (drug), Lubricating Eye Drops (drug), Prednisolone acetate ophthalmic suspension 1% eye drops (drug), Brimonidine tartrate ophthalmic solution eye drops (drug)
Dates
Started 2024-07-29; completion 2027-02
Results posted
Not yet

The purpose of this study is to evaluate the incidence rate and severity of prespecified mirvetuximab soravtansine (MIRV)-related ocular treatment-emergent adverse events (TEAEs) and assess prophylaxis strategies in all participants (symptomatic and asymptomatic) undergoing prospective ophthalmic evaluation with recurrent ovarian cancer (participants with either platinum-sensitive ovarian cancer \[PSOC\] or platinum-resistant ovarian cancer \[PROC\]) with high folate receptor alpha (FRα) expression.

From ClinicalTrials.gov, last updated 2026-08-21. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $320,889 in research payments for this study in 2025 (27 payments).

Products named: Elahere

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.