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)

Фаза 3 Завершено NCT04662710

ЗаболеваниеAdvanced/Metastatic Gastroesophageal Adenocarcinoma
ФазаФаза 3
СпонсорMerck Sharp & Dohme LLC
СтатусЗавершено
Участники895 участн.
ВмешательствоPembrolizumab, Lenvatinib, Oxaliplatin, Capecitabine, Leucovorin (or Levoleucovorin)
Дата начала30.12.2020
Дата завершения29.10.2024
Публикация результатов28.11.2025

Кратко

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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