Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT03950609

Lenvatinib and Everolimus in Treating Patients With Advanced, Unresectable Carcinoid Tumors

A Phase II Study of Lenvatinib in Combination With Everolimus in Patients With Advanced Carcinoid Tumors

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
36 (actual)
Sponsor
M.D. Anderson Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This phase II trial studies how well lenvatinib and everolimus work in treating patients with carcinoid tumors that have spread to other places in the body (advanced) and cannot be removed by surgery (unresectable). Lenvatinib and everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Detailed description

PRIMARY OBJECTIVE: I. To estimate the Response Evaluation Criteria in Solid Tumors (RECIST) (per version 1.1) objective response rate of lenvatinib in combination with everolimus among patients with advanced carcinoid tumors. SECONDARY OBJECTIVES: I. To evaluate the progression free survival duration of lenvatinib in combination with everolimus among patients with advanced carcinoids. II. To evaluate the safety and tolerability of lenvatinib in combination with everolimus among patients with advanced carcinoid tumors. EXPLORATORY OBJECTIVES: I. To determine clinic benefit rate at 6 months (defined as complete response plus partial response plus stable disease) with lenvatinib + everolimus among patients with advanced carcinoid tumors. II. To determine early CgA and neuron-specific enolase (NSE) response rates. OUTLINE: Patients receive lenvatinib orally (PO) daily and everolimus PO daily on days 1-28. Treatments repeat every 28 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up at 30 days.

Conditions

Interventions

TypeNameDescription
DRUGEverolimusGiven PO
DRUGLenvatinibGiven PO

Timeline

Start date
2019-07-30
Primary completion
2028-03-30
Completion
2028-03-30
First posted
2019-05-15
Last updated
2026-03-19

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03950609. Inclusion in this directory is not an endorsement.