CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 357 enrolled
Drug / intervention
Lenvatinib +1 moredrug
Likely dose
Pembrolizumab 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02501096
NCT02501096Phase 2Completed

A Multicenter, Open-Label Phase 1b/2 Trial of Lenvatinib (E7080) Plus Pembrolizumab in Subjects With Selected Solid Tumors

Eisai Inc.·interventional·Posted Jul 17, 2015·Updated Jul 20, 2023

In Brief

A Phase 2 clinical trial evaluating Lenvatinib and Pembrolizumab for Tumors. Completed, enrolled 357 participants across 64 sites in 3 countries.

Detailed Summary

This is an open-label Phase 1b/2 trial of lenvatinib (E7080) plus pembrolizumab in participants with selected solid tumors. Phase 1b will determine and confirm the maximum tolerated dose (MTD) for lenvatinib in combination with 200 milligrams (mg) (intravenous \[IV\], every 3 weeks \[Q3W\]) pembrolizumab in participants with selected solid tumors (i.e. non-small cell lung cancer, renal cell carcinoma, endometrial carcinoma, urothelial carcinoma, squamous cell carcinoma of the head and neck, melanoma or leiomyosarcoma). Phase 2 (Expansion) will evaluate the safety and efficacy of the combination in 7 cohorts at the MTD from Phase 1b (lenvatinib 20 mg/day orally + pembrolizumab 200 mg Q3W, IV).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTumors
CountriesNorway, Spain, United States

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedJul 17, 2015
Enrollment StartJul 22, 2015
Primary CompletionAug 18, 2020
Study CompletionJul 11, 2022
TodayJul 2, 2026
Enrollment to primary: 5.1 yearsPosted 11.0 years ago

Interventions

Lenvatinibdrug

Lenvatinib will be administered with water orally once a day (with or without food) continuously in 21-day treatment cycle.

Pembrolizumabdrug

Pembrolizumab will be administered as a dose of 200 mg Q3W, IV in 21-day treatment cycle.