About this trial
There is a lack of strategies for patients who progress after responding to PD-1/l-1 in melanoma. High expression of Nectin4 in skin and melanomas may serve as a new target in advanced melanomas. The combination of enfortumab/vedotin (EV) and pembrolizumab has shown synergistic effect in various solid tumors. Enfortumab vedotin and pembrolizumab may have a dual effect on clinical outcomes.
PLUGIN is a multicenter, non-randomized open-label, 2-cohort, phase 2 study to evaluate the ORR of pembrolizumab in combination with enfortumab vedotin (EV) in previously treated participants with unresectable stage III or IV melanoma and disease progression on standard therapy.
The primary objective is evaluate the efficacy of enfortumab/vedotin and pembrolizumabplus pembrolizumab in advanced melanoma.
Hypothesis: 1) High expression of Nectin4 in skin and melanomas may serve as a new target in advanced melanomas; 2)EV+Pembrolizumab has shown synergistic effect in various solid tumors; 3) There is a lack of strategies for patients who respond to PD1-mAbs in melanoma.
Primary Endpoint: Objective Response Rate (ORR) as assessed by the investigator according RECIST 1.1
A total of 60 patients will be enrolled in this study to evaluate efficacy and outcomes in two different cohorts:
Cohort 1: patients who did not have BRAF mutation V600E and had disease progression on immune (IO) therapy.
Cohort 2, patients with activating BRAF mutations, must have progressed on IO therapy and BRAF/MEKi
Eligibility criteria
Qualifiers
Male/female participants who are at least 18 years of age on the day of signing informed consent with histologically confirmed diagnosis of unresectable or metastatic melanoma will be enrolled in this study.
Participants must have measurable disease by investigator assessment according to RECIST v1.1 Participants with prior definitive radiation therapy must have measurable disease per RECIST v1.1 that is outside the radiation field or has demonstrated unequivocal progression since completion of radiation therapy.
Not a woman of childbearing potential (WOCBP) as defined in Appendix 3. OR
WOCBP should remain on contraception for 12 months after the last dose of EV or 4 months after pembrolizumab, whichever occurs last.
Disqualifiers
Participants who have previously received enfortumab vedotin or other MMAE-based ADCs.
Has received prior systemic anti-cancer therapy including investigational agents within 4 weeks prior to the scheduled date of starting the study treatment.
Has received prior radiotherapy within 2 weeks of start of study intervention or radiation-related toxicities requiring corticosteroids.
Has received a live vaccine or live-attenuated vaccine within 30 days before the first dose of study intervention. Administration of killed vaccines is allowed.
Trial design
Treatments tested in this trial
- enfortumab vedotin
- pembrolizumab
Treatment groups
Sponsors and collaborators
Grupo Español Multidisciplinar de Melanoma
Lead sponsor
Merck Sharp & Dohme LLC
Collaborator
Astellas Pharma Inc
Collaborator