Conditions
Melanoma
Clinical Trials
The primary purpose of this study is to compare pembrolizumab/vibostolimab to pembrolizumab with respect to recurrence-free survival (RFS). The primary hypothesis is that pembrolizumab/vibostolimab is superior to pembrolizumab with respect to RFS as assessed by the investigator in participants with high-risk resected Stage IIB, IIC, III and IV melanoma.
CLINICALTRIALS.GOV IDENTIFIER
NCT05665595
EudraCT Number
2022-501417-31-00
EU CT Number
2022-501417-31-00
When you talk with your doctor or clinical trial team member, please have the trial identifier number available.
Only a qualified healthcare professional can determine if you are eligible to take part in a clinical trial. However, this information may be useful in starting a conversation with your doctor.
Conditions
Melanoma
Age Range
12+
Sex
All
All patients who enroll in the trial will be randomized to receive 1 of 2 adjuvant treatments while on the study.
50% will receive MK-7684A*
50% will receive Pembrolizumab
*MK-7684A is a combination of 2 investigational study drugs: MK-7684 and Pembrolizumab
In Phase 3 trials, researchers try to find out if a treatment works in a large number of people, usually about 1,000 to 5,000 participants who have the health condition the treatment is intended to treat. In vaccine trials, the participants may be healthy or have diseases or conditions. Phase 3 trials may happen in a doctor’s office, a clinic, or a hospital.
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If you think this clinical trial might be a good fit and you are interested in taking part, take the next step to see if you are eligible.
If you are considering joining a clinical trial, first learn as much as you can about:
Talk to your doctor about the clinical trial before you decide to join.
Read our “What to Consider” page for more questions to ask and think about