Botensilimab and Balstilimab Optimization in Colorectal Cancer (BBOpCo)

Botensilimab and Balstilimab Optimization in Colorectal Cancer (BBOpCo)

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Purpose of this Study

We are doing this study to see if a pair of experimental drugs called botensilimab and balstilimab are safe and effective options for colorectal cancer.

Who Can Participate?

Eligibility

Adults ages 18+ who:
  • Are diagnosed with unresectable or metastatic colorectal cancer
  • Do not have metastases to the liver, bone, or brain
  • Have not received prior therapy for their current cancer
For more information, contact the study team at justinemae.flores@duke.edu.

Age Range

18-110

Sex/Genders

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

What is Involved?

Description

If you choose to join this study, you will:
  • Get the study drug balstilimab by IV once every 2 weeks for up to 2 years
  • Get the study drug botensilimab by IV on weeks 1, 7, 13, and 19 while you are getting balstilimab
  • Receive standard anti-cancer drugs if your cancer does not improve on the study regimen
  • Have your tumor biopsied
  • Have blood draws
  • Have regular CT or MRI scans

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

No

Spanish Materials Available

No

Study Details

Full Title

Botensilimab and Balstilimab Optimization in Colorectal Cancer (BBOpCo)

Principal Investigator

Nicholas
DeVito

Protocol Number

PRO00115311

NCT ID

NCT06268015

Phase

II

Enrollment Status

Open to Enrollment