BENITIONSClinical Trial Intelligence

Efficacy and Safety of Lenvatinib (E7080/MK-7902) Plus Pembrolizumab (MK-3475) Plus Chemotherapy in Participants With Advanced/Metastatic Gastroesophageal Adenocarcinoma (MK-7902-015/E7080-G000-321/LEAP-015)

Phase 3 Completed NCT04662710

ConditionAdvanced/Metastatic Gastroesophageal Adenocarcinoma
PhasePhase 3
SponsorMerck Sharp & Dohme LLC
StatusCompleted
Enrollment895 participants
InterventionsPembrolizumab, Lenvatinib, Oxaliplatin, Capecitabine, Leucovorin (or Levoleucovorin)
Start dateDec 30, 2020
Completion dateOct 29, 2024
Results postedNov 28, 2025

Summary

The purpose of this study is to assess the efficacy and safety of lenvatinib (E7080/MK-7902) plus pembrolizumab (MK-3475) plus chemotherapy compared with chemotherapy alone in participants with advanced/metastatic gastroesophageal cancer. The primary study hypotheses are that lenvatinib plus pembrolizumab plus chemotherapy is superior to chemotherapy alone for both overall survival (OS) and progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) as assessed by blinded independent central review (BICR), in participants with programmed cell death-ligand 1 (PD-L1) Combined Positive Score (CPS) ≥1 and in all participants.

Part 1: Number of Participants With Dose Limiting Toxicities (DLTs)

Up to ~21 days · Participants

Part 1 : Lenvatinib + Pembrolizumab + Chemotherapy2 Participants

Part 1: Number of Participants With Adverse Events (AEs)

Up to ~44 months · Participants

Safety Run-In: Lenvatinib + Pembrolizumab + Chemotherapy15 Participants

Part 1: Number of Participants Who Discontinued Study Treatment Due to an AE

Up to ~29 months · Participants

Safety Run-In: Lenvatinib + Pembrolizumab + Chemotherapy5 Participants

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