drugset / Trial / NCT04447755

A Study of Lenvatinib (MK-7902) in Pediatric Participants With Relapsed or Refractory Solid Malignancies (MK-7902-013/E7080)

NCT04447755 ↗

Phase 2 Completed 127 enrolled Merck Sharp & Dohme LLC Eisai Inc. · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The main purpose of this study is to evaluate the antitumor activity and safety of lenvatinib (MK-7902/E7080) in children, adolescents, and young adults with relapsed or refractory solid malignancies after administration. Participants were enrolled into Ewing sarcoma (EWS), rhabdomyosarcoma (RMS), high-grade glioma (HGG), diffuse midline glioma, medulloblastoma, ependymoma, and Other Solid Tumors Excluding Osteosarcoma, diffuse midline glioma, medulloblastoma, and ependymoma cohorts.

Timeline

Start
2020-07-30
Primary completion
2022-09-16
Completion
2025-02-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenvatinib Small molecule 14 mg/m2 Oral