AFT-50 EndoMAP Targeted Agents and/or Immunotherapy with Atezolizumab for Endometrial Cancer

AFT-50 EndoMAP Targeted Agents and/or Immunotherapy with Atezolizumab for Endometrial Cancer

Purpose of this Study

We are doing this study to find out if certain experimental drug combinations are safe and effective options for people who have recurrent or persistent endometrial cancer (cancer that has come back after treatment or does not respond to treatment).

Who Can Participate?

Eligibility

Adults ages 18+ who:<ul>
<li>Are diagnosed with endometrial cancer</li>
<li>Did not respond to previous treatment or had their cancer return after treatment</li>
<li>Have not received more than 2 lines of previous therapy (can include chemoradiation, chemotherapy and/or biologic therapy, or maintenance/consolidation therapy - hormonal therapies like aromatase inhibitors or tamoxifen do not count as a line of therapy)</li></ul>
For more information about 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
Transgender female
Looking for Healthy Participants
No

What is Involved?

If you choose to join this study, you will be assigned a specific study regimen based on specific biomarkers we find in a sample of your tumor. Depending on our findings, you will get one of the following study drug regimens:<ul>
<li>Atezolizumab + Bevacizumab doublet</li>
<li>Atezolizumab + Ipatasertib doublet</li>
<li>Atezolizumab + Talazoparib doublet</li>
<li>Atezolizumab + Trastuzumab Emtansine</li>
<li>Atezolizumab and Tiragolumab</li>
<li>Inavolisib + Letrozole doublet</li></ul>

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

No

Spanish Materials Available

No

Study Details

Full Title

A Phase IB/II Multi-Cohort Study of Targeted Agents with Atezolizumab for Patients with Recurrent or Persistent Endometrial Cancer

Principal Investigator

Angeles
Secord

Protocol Number

PRO00107981

NCT ID

NCT04486352

Phase

I/II

Enrollment Status

Open to Enrollment