Purpose of this Study
We are doing this study to compare the safety and effects of stopping the standard melanoma treatments of nivolumab + pembrolizumab or nivolumab + relatlimab at different times. We hope this study will help us discover certain markers from imaging and biopsies that can signal when it is the appropriate time to stop therapy.
Who Can Participate?
Eligibility
Adults ages 18+ who:
- Are diagnosed with advanced melanoma that is unresectable stage IIIB-IV; OR are diagnosed with mucosal melanoma that is unresectable stage III or regional/distant metastatic disease
- Have been receiving standard anti-PD-1 therapy for at least 1 year
- Do not have any known inability to take any of the study drugs (nivolumab + pembrolizumab or nivolumab + relatlimab)
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 have certain procedures done to determine when you should stop using your current therapy. The steps that will be taken are as follows:
- After you hit the 1-year mark of taking your standard therapy, we will schedule you to have a PET/CT scan. If there is no evidence of disease on this scan, you will stop the therapy. If there is evidence that disease might still be present, we will schedule you for a biopsy.
- If you have the biopsy done, the results will guide what happens next. If there are no active cancer cells detected in the biopsy, you will discontinue your therapy. If the biopsy is positive for cancer cells, you will continue your current therapy for at least 1 more year.
Locations
Duke University Hospital
Duke Raleigh Hospital
Visit Timing
Weekdays
Compensation
No
Spanish Materials Available
Yes
Study Details
Full Title
EA6192: A Phase II Study of Biomarker Driven Early Discontinuation of Anti-PD-1 Therapy in Patients with Advanced Melanoma (PET-Stop)
Principal Investigator
Riddhishkumar
Shah
Protocol Number
PRO00113243
NCT ID
NCT04462406
Phase
II
Enrollment Status
Open to Enrollment