drugset / Trial / NCT05282901

Efficacy and Safety of Pembrolizumab in Combination With Lenvatinib in Metastatic Uveal MElanoma Patients (PLUME)

NCT05282901 ↗

Phase 2 Active not recruiting 51 enrolled Institut Curie Merck Sharp & Dohme LLC · collab
NaSingle-groupOpen-labelTreatment

Summary

Because we suspect that the benefit of anti-PD-1 in metastatic UM patients could vary according to previous exposure to Tebentafusp (better efficacy of anti-PD-1 after Tebentafusp), the combination of pembrolizumab and lenvatinib will be assessed in two independent cohorts: cohort 1 with Tebentafusp-naive patients, and cohort 2 with patients previously treated by Tebentafusp. The study is a monocentric, phase II trial with a single-arm of treatment in each cohort. Liver MRI and chest-abdomen-pelvis CT will be performed every 9 weeks until progressive disease (PD), followed by a Follow-up visit within 28 days after last treatment intake. Survival status will be registered after patient discontinuation.

Timeline

Start
2022-07-07
Primary completion
2026-10-30
Completion
2026-11-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenvatinib Small molecule — —
Subject Pembrolizumab Monoclonal antibody 25 mg Intravenous

Indications