RecruitingPhase 2NCT03832361

Evaluation of Mirvetuximab Soravtansine (IMGN853) in Women With Folate Receptor-α Positive Endometrial Cancer

A Phase II Evaluation of the Safety and Efficacy of Mirvetuximab Soravtansine (IMGN853) in Women With Folate Receptor-α Positive Persistent or Recurrent Endometrial Cancer


Sponsor

Alessandro Santin

Enrollment

50 participants

Start Date

Jul 15, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the activity and safety profile of mirvetuximab soravtansine (IMGN853) in patients with type II endometrial cancers that overexpress folate receptor alpha (FRα).


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 100 Years

Plain Language Summary

Simplified for easier understanding

This study is evaluating a targeted drug called mirvetuximab soravtansine in women whose uterine (endometrial) cancer has come back or kept growing after earlier treatments, focusing specifically on tumors that have a certain protein (folate receptor alpha) on their surface. **You may be eligible if...** - You are a woman with persistent or recurrent endometrial (uterine) cancer confirmed by imaging - Your tumor is a specific type: uterine serous carcinoma, grade 2 or 3 adenocarcinoma, carcinosarcoma, or clear cell carcinoma - Your tumor tests positive for a protein called folate receptor alpha - You have received no more than 3 prior lines of treatment for your recurrent cancer - You are in generally good health (ECOG performance status 0 or 1) - Your heart, liver, and kidney function are adequate **You may NOT be eligible if...** - You have not had measurable disease on imaging - You have received more than 3 prior treatment regimens for recurrent disease - You have previously been treated with folate receptor-targeting drugs - Your side effects from prior treatments have not resolved adequately Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIMGN853

IMGN853 6 mg/kg intravenously every 3 weeks until disease progression


Locations(1)

Smilow Cancer Hospital at Yale New Haven

New Haven, Connecticut, United States

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NCT03832361


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