Clinical Trials Directory

Trials / Completed

CompletedNCT03829332

Efficacy and Safety Study of Pembrolizumab (MK-3475) With or Without Lenvatinib (MK-7902/E7080) in Adults With Programmed Cell Death-Ligand 1 (PD-L1)-Positive Treatment-naïve Nonsmall Cell Lung Cancer (NSCLC) (MK-7902-007/E7080-G000-314/LEAP-007)

A Phase 3, Randomized, Double-blind Trial of Pembrolizumab (MK-3475) With or Without Lenvatinib (E7080/MK-7902) in Participants With Treatment-naïve, Metastatic Nonsmall Cell Lung Cancer (NSCLC) Whose Tumors Have a Tumor Proportion Score (TPS) Greater Than or Equal to 1% (LEAP-007)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
623 (actual)
Sponsor
Merck Sharp & Dohme LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the safety and efficacy of pembrolizumab (MK-3475) combined with lenvatinib (MK-7902/E7080) compared to pembrolizumab alone (with placebo for lenvatinib) in treatment-naïve adults with no prior systemic therapy for their metastatic non-small cell lung cancer (NSCLC) whose tumors have a programmed cell death-ligand 1 (PD-L1) Tumor Proportion Score (TPS) greater than or equal to 1%. The primary study hypotheses are that: 1) the combination of pembrolizumab and lenvatinib is superior to pembrolizumab alone as assessed by Progression-free Survival (PFS) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1); and 2) the combination of pembrolizumab and lenvatinib is superior to pembrolizumab alone as assessed by Overall Survival (OS).

Detailed description

As of 30-Jul-2021, active participants, investigator, and sponsor personnel or delegate(s) involved in the treatment administration or clinical evaluation of the participants will be unblinded. Participants will discontinue lenvatinib and placebo, and participants who remain on treatment will receive open-label pembrolizumab only.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPembrolizumabIV infusion
DRUGLenvatiniboral capsule
DRUGPlacebo for lenvatiniboral capsule

Timeline

Start date
2019-03-13
Primary completion
2021-05-19
Completion
2024-04-24
First posted
2019-02-04
Last updated
2026-02-19
Results posted
2022-06-02

Locations

162 sites across 19 countries: United States, Australia, Canada, China, Colombia, Estonia, France, Hungary, Israel, Italy, Japan, Malaysia, Mexico, Poland, Russia, South Korea, Taiwan, Turkey (Türkiye), Ukraine

Regulatory

Source: ClinicalTrials.gov record NCT03829332. Inclusion in this directory is not an endorsement.