NRG-GY025 Endometrial Cancer

NRG-GY025 Endometrial Cancer

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Purpose of this Study

We are doing this study to find out if the study drugs nivolumab and ipilimumab are a safe and effective option for people who have endometrial cancer that does not respond to standard treatment and/or has spread to other parts of the body. We want to compare the results of using these 2 drugs together versus using nivolumab alone.

Who Can Participate?

Eligibility

Women ages 18+ who:
  • Are diagnosed with recurrent or metastatic endometrial cancer
  • Have not received more than 2 previous lines of therapy
For more information about who can join this study, contact the study team at nick.jeffries@duke.edu.

Age Range

18-110

Sex/Genders

Female (cisgender)
Non-binary or gender fluid
Transgender male
Looking for Healthy Participants
No

What is Involved?

Description

If you decide to participate in this study, you will get a random assignment (like a coin flip) to 1 of 2 groups:
  • Group 1: You will get the study drugs nivolumab and ipilimumab. You will get the nivolumab through a vein in the arm or through a port on the first day of each cycle. Each cycle lasts 3 weeks. You will also get the drug ipilimumab through a vein in the arm or through a port on the first day of every other cycle (every 6 weeks).
  • Group 2: You will receive the study drug nivolumab. You will get this drug through a vein in the arm or through a port on the first day of each cycle.

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

No

Spanish Materials Available

Yes

Study Details

Full Title

NRG-GY025: A Randomized Phase II Trial of Nivolumab and Ipilimumab compared to Nivolumab Monotherapy in Patients with Deficient Mismatch Repair System Recurrent Endometrial Carcinoma--Safety Lead-in Portion
(NCT # 05112601)

Principal Investigator

Angeles
Secord

Protocol Number

PRO00113684

NCT ID

NCT05112601

Phase

II

Enrollment Status

Open to Enrollment