CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 481 enrolled
Drug / intervention
Favezelimab +7 morebiological
Likely dose
Not stated in 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/NCT02720068
NCT02720068Phase 1Completed

A Phase 1 Trial of MK-4280 as Monotherapy and in Combination With Pembrolizumab With or Without Chemotherapy or Lenvatinib (E7080/MK-7902) in Subjects With Advanced Solid Tumors

Merck Sharp & Dohme LLC·interventional·Posted Mar 25, 2016·Updated May 30, 2025

In Brief

A Phase 1 clinical trial evaluating Favezelimab, Pembrolizumab, and 6 other interventions for Neoplasms. Completed, enrolled 481 participants.

Detailed Summary

This is a safety and pharmacokinetics study of favezelimab as monotherapy and in combination with pembrolizumab AND favezelimab/pembrolizumab as monotherapy in adults with metastatic solid tumors for which there is no available therapy which may convey clinical benefit. Part A of this study is a dose escalation design in which participants receive favezelimab as monotherapy or favezelimab in combination with pembrolizumab. Part B is a dose confirmation design to estimate the recommended Phase 2 dose (RP2D), as determined by dose-limiting toxicity, for favezelimab in combination with pembrolizumab or pembrolizumab and lenvatinib in participants with advanced solid tumors. Part B will also assess the efficacy of favezelimab as monotherapy; favezelimab in combination with pembrolizumab with and without chemotherapy; favezelimab in combination with pembrolizumab and lenvatinib; and favezelimab/pembrolizumab as monotherapy in expansion cohorts. Participants who have completed the initial course of treatment and have investigator-determined progressive disease may be eligible for a second course of an additional 17 cycles of study treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNeoplasms
Countries--
Collaborators--

Timeline

Phase 1CompletedFinished
20162017201820192020202120222023202420252026
First PostedMar 25, 2016
Enrollment StartMay 2, 2016
Primary CompletionMar 15, 2024
TodayJul 2, 2026
Enrollment to primary: 7.9 yearsPosted 10.3 years ago

Interventions

Favezelimabbiological

IV infusion

Pembrolizumabbiological

IV infusion

Oxaliplatindrug

IV infusion

Irinotecandrug

IV infusion

Leucovorin (Calcium Folinate)drug

IV infusion

Fluorouracil [5-FU]drug

IV infusion

Favezelimab/Pembrolizumabbiological

IV infusion

Lenvatinibdrug

Oral