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Completed Phase 3 Interventional Results available

A Study of Mirvetuximab Soravtansine in Platinum-Resistant, Advanced High-Grade Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancers With High Folate Receptor-Alpha Expression

ClinicalTrials.gov ID: NCT04296890

Public ClinicalTrials.gov record NCT04296890. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 6:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

SORAYA: A Phase 3, Single Arm Study of Mirvetuximab Soravtansine in Platinum-Resistant, Advanced High-Grade Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancers With High Folate Receptor-Alpha Expression

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is designed to evaluate the efficacy and safety of mirvetuximab soravtansine (MIRV) in participants with platinum-resistant high-grade serous epithelial ovarian cancer, primary peritoneal, or fallopian tube cancer, whose tumors express a high-level of Folate Receptor-Alpha (FRα). Participants will be, in the opinion of the Investigator, appropriate for single-agent therapy for their next line of therapy. All participants will receive single-agent MIRV at 6 mg/kg adjusted ideal body weight administered on Day 1 of every 3-week cycle.

Study identification

NCT ID
NCT04296890
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ImmunoGen, Inc.
Industry
Enrollment
106 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 23, 2020 (Actual)
Primary completion
Nov 16, 2021 (Actual)
Completion
Nov 16, 2022 (Actual)
Last update posted
Aug 7, 2024

2020 – 2022

United States locations

U.S. sites
34
U.S. states
20
U.S. cities
32
Facility City State ZIP Site status
Arizona Oncology Associates Phoenix Arizona 85016 —
City of Hope Medical Center Duarte California 91010 —
California Cancer Associates (cCARE) Fresno California 93720 —
Stanford School of Medicine Palo Alto California 94394 —
California Pacific Medical Center Research Institute San Francisco California 94109 —
Rocky Mountain Cancer Centers Littleton Colorado 80120 —
Sarasota Memorial Health Care System Sarasota Florida 34239 —
Florida Cancer Specialists Panhandle Tallahassee Florida 32308 —
University of South Florida Tampa Florida 33606 —
Florida Cancer Specialists Research West Palm Beach Florida 33401 —
Northside Hospital Atlanta Georgia 30342 —
Hinsdale Hospital Hinsdale Illinois 60521 —
St. Vincent Gynecologic Oncology Indianapolis Indiana 46260 —
University of Kansas Cancer Center Westwood Kansas 66205 —
Norton Cancer Institute Louisville Kentucky 40207 —
Women's Cancer Center Covington Louisiana 70433 —
Maryland Oncology Hematology, P.A. Rockville Maryland 20850 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Midwest Oncology Associates/Sarah Cannon Kansas City Missouri 64132 —
Center of Hope at Renown Medical Center Reno Nevada 89502 —
Holy Name Medical Center Teaneck New Jersey 07666 —
Mount Sinai Health System New York New York 10029 —
Memorial Sloan-Kettering Cancer Center New York New York 10065 —
Sarah Cannon Research Institute / Tennessee Oncology, PLLC Nashville Tennessee 37203 —
Texas Oncology-Austin Central Austin Texas 78731 —
Texas Oncology, P.A. - Fort Worth Cancer Center Fort Worth Texas 76104 —
Texas Oncology, P.A. - McAllen McAllen Texas 78503 —
Texas Oncology, P.A. - Sugar Land Sugar Land Texas 77479 —
USOR: Texas Oncology - The Woodlands, Gynecologic Oncology The Woodlands Texas 77380 —
Texas Oncology, P.A. - Tyler Tyler Texas 75702 —
Kadlec Clinic Hematology and Oncology Kennewick Washington 99336 —
University of Wisconsin Carbone Cancer Center Madison Wisconsin 53792 —
Froedtert and the Medical College of Wisconsin Department of Obstetrics & Gynecology Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04296890, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 7, 2024 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04296890 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →