Pfizer COVID-19 vaccine appointments are available to our patients. Sign up for Connect today to schedule your vaccination.

A Phase 3, Randomized, Active-controlled, Open-label, Multicenter Study to Compare the Efficacy & Safety of MK-2870 Monotherapy Vs Treatment of Physician’s Choice in Endometrial Cancer Participants Who Received Prior Platinum-based Chemo & Immunotherapy

Clinical Trial Details

This trial is testing the drug MK-2870 in people with endometrial cancer that has already been treated with certain types of drugs. This trial will compare MK-2870 to 2 standard chemotherapies used to treat endometrial cancer: doxorubicin and paclitaxel. 

The purpose of this trial is to test the safety MK-2780, see how well it works compared to the 2 standard chemotherapies, see if participants who get MK-2870 live longer compared to those who get a standard chemotherapy, and see if participants who get MK-2870 have a better quality of life compared to those who get who get a standard chemotherapy.
   
MK-2870 is experimental, which means it has not been approved by any national authority such as the U.S. Food and Drug Administration (FDA). Doxorubicin and paclitaxel are approved by the FDA.

Participants will be randomized into one of two groups. Randomization is like flipping a coin and there is a 50/50 chance of being assigned to either group. Group one will get MK-2870 and group 2 will get doxorubicin or paclitaxel. All treatments are given via an intravenous (IV) infusion.

Both groups will need to come in for trial visits. The frequency of visits depends on which group the participant is assigned to and if in group 2, which drug they are assigned to.

Total study participation is expected to last approximately 4 years. 

Key Eligibility: 
  1. Open to women above the age of 18 who have been diagnosed with endometrial carcinoma or carcinosarcoma. 
  2. Participant must not have neuroendocrine tumors or endometrial sarcoma and must not be currently pregnant or breast feeding. 

   
Detailed eligibility will be reviewed when you contact the study team.

Study contact by location

Brooklyn

Contact(s)

Kate Santoso
929-470-9507
bnk9002@med.cornell.edu

Primary Investigator(s)

Protocol ID(s)

Weill Cornell Medicine IRB #:

2402027130

ClinicalTrials.gov:

NCT06132958

Sponsor:

MK-2870-005/ENGOT-en23/GOG-095

Status

Not Yet Recruiting

Age Group

Adult

Sponsor