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Study identifier: NCT06890338 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Assess Anti-Tumor Activity of Intravenously (IV) Infused Carboplatin With Mirvetuximab Soravtansine in Participants With Newly Diagnosed Folate Receptor Alpha (FRα)Expressing Advanced-Stage Serous Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer.

Condition: Epithelial Ovarian Cancer · Fallopian Tube Cancer · Primary Peritoneal Cancer  ·  Sponsor: AbbVie

PhasePhase 2
Planned participants140
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess the safety and efficacy of neoadjuvant carboplatin and mirvetuximab soravtansine in participants with folate receptor alpha (FRα) -expressing advanced-stage serous epithelial ovarian, fallopian tube or primary peritoneal cancer (EOC). Mirvetuximab Soravtansine (MIRV) is an investigational antibody drug conjugate designed to selectively kill cancer cells. The antibody (protein) part of MIRV targets tumors by delivering a cell-killing drug to cancer cells carrying a protein called folate receptor alpha (FRα). This is a single arm study in adult participants with advanced-stage Fédération Internationale de Gynécologie et d'Obstétrique (FIGO) III-IV FRα-expressing serous EOC. Around 140 participants will be enrolled in the study at approximately 80 sites in the United States. Participants will receive intravenous infusion of MIRV in combination with carboplatin on day 1 of each cycle, every 21 days for up to 6 - 9 Cycles. The total study duration will be approximately 3 years . There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic and may require frequent medical assessments, blood tests, and scans.

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (67)

University of Alabama at Birmingham (UAB) Hospital /ID# 274793Birmingham, Alabama, United StatesRecruiting
Usa Mitchell Cancer Institute /ID# 276022Mobile, Alabama, United StatesRecruiting
University of California Los Angeles Medical Center /ID# 274566Los Angeles, California, United StatesRecruiting
Scripps Md Anderson - Prebys Cancer Center /ID# 276891San Diego, California, United StatesRecruiting
California Pacific Medical Center - Van Ness Campus /ID# 275329San Francisco, California, United StatesRecruiting
Ridley Tree Cancer Center /ID# 275219Santa Barbara, California, United StatesActive Not Recruiting
Danbury Hospital, Western Connecticut Health Network /ID# 274783Danbury, Connecticut, United StatesRecruiting
Yale University School of Medicine /ID# 275794New Haven, Connecticut, United StatesRecruiting
Norwalk Hospital /ID# 274561Norwalk, Connecticut, United StatesRecruiting
Jupiter Medical Center /ID# 276616Jupiter, Florida, United StatesRecruiting
Mount Sinai Medical Center /ID# 274868Miami Beach, Florida, United StatesRecruiting
Rush Md Anderson Cancer Center /ID# 274926Chicago, Illinois, United StatesRecruiting

+ 55 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06890338