MK-2870-005 MK-2870 Monotherapy Versus Treatment of Physician's Choice in Endometrial Cancer

MK-2870-005 MK-2870 Monotherapy Versus Treatment of Physician's Choice in Endometrial Cancer

Purpose of this Study

We are doing this study to find out if an experimental drug called MK-2870 (the study drug) is an option for patients with endometrial cancer. We want to know how well it works compared to standard chemotherapy.

Who Can Participate?

Eligibility

Adults ages 18+ who:<ul>
<li>Are diagnosed with endometrial carcinoma or carcinosarcoma</li>
<li>Have received previous treatment with platinum-based chemotherapy and anti-PD-1/anti-PD-L1 therapy (given either together or separately)</li>
<li>Are not pregnant or breastfeeding</li></ul>
For more information about who can join this study, contact the study team at <a href= "mailto: william.s.andrews@duke.edu";> william.s.andrews@duke.edu.</a>

Age Range

18-110

Sex/Genders

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

What is Involved?

If you choose to join this study, you will get a random assignment (like a coin flip) to either take the study drug or a combination of doxorubicin and paclitaxel (the standard chemotherapy regimen).<ul>
<li>If you are assigned the study drug, you will get a dose of it every 2 weeks.</li>
<li>If you are assigned to get standard chemotherapy, you will get a dose of doxorubicin once every 3 weeks. You will also get paclitaxel once per week for 3 out of 4 weeks.</li></ul>
You will continue to receive your assigned study drug regimen as long as you benefit from it. You may be in the study for up to 4 years.

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

No

Spanish Materials Available

No

Study Details

Full Title

A Phase 3, Randomized, Active-controlled, Open-label, Multicenter Study to
Compare the Efficacy and Safety of MK-2870 Monotherapy Versus Treatment of
Physician’s Choice in Participants With Endometrial Cancer Who Have Received Prior
Platinum-based Chemotherapy and Immunotherapy (MK-2870-005/ENGOT-en23/GOG-
3095)

Principal Investigator

Angeles
Secord

Protocol Number

PRO00114641

NCT ID

NCT06132958

Phase

III

Enrollment Status

Open to Enrollment