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Completed Phase 2 Interventional Results available

A Study of Emibetuzumab in Non Small Cell Lung Cancer (NSCLC) Participants

ClinicalTrials.gov ID: NCT01900652

Public ClinicalTrials.gov record NCT01900652. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 4:13 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-Label Phase 2 Study Evaluating LY2875358 Plus Erlotinib and LY2875358 Monotherapy in MET Diagnostic Positive NSCLC Patients With Acquired Resistance to Erlotinib

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary purpose of this study is to evaluate the efficacy of the study drug known as LY2875358, administered alone or in combination with a second drug named Erlotinib, in participants affected by a defined type of lung cancer (MET biomarker diagnostic positive Non-Small-Cell Lung Cancer) that experienced a disease progression during the most recent treatment with Erlotinib.

Study identification

NCT ID
NCT01900652
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
111 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2013 (Type not available)
Primary completion
Feb 2015 (Actual)
Completion
Mar 2016 (Actual)
Last update posted
Sep 18, 2019

2013 – 2016

United States locations

U.S. sites
32
U.S. states
21
U.S. cities
31
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
University of California - San Diego La Jolla California 92037 —
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. Los Angeles California 90048 —
University of California, Davis - Health Systems Sacramento California 95817 —
UCLA Santa Monica California 90404 —
University of Colorado Health Sciences Center Aurora Colorado 80045 —
Georgetown University Medical Center IRB Washington D.C. District of Columbia 20007 —
Florida Cancer Specialists Fort Myers Florida 33916-2233 —
Florida Cancer Specialists St. Petersburg Florida 33705 —
H Lee Moffitt Cancer Center Tampa Florida 33612 —
Northeast Georgia Cancer Care, LLC Athens Georgia 30607 —
Emory University Atlanta Georgia 30322 —
University of Iowa Hospital Iowa City Iowa 52242 —
University of Kansas Medical Center Westwood Kansas 66205 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Karmanos Cancer Institute Detroit Michigan 48201 —
Mayo Clinic Rochester Minnesota 55905 —
Washington University Medical Center St Louis Missouri 63110 —
Billings Clinic Research Center Billings Montana 59101 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 —
Columbia University New York New York 10032 —
Carolinas Medical Center Charlotte North Carolina 28204 —
Oncology Hematology Care Inc Cincinnati Ohio 45242 —
Portland VA Medical Center Portland Oregon 97213 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
Tennessee Oncology PLLC Chattanooga Tennessee 37404 —
The West Clinic Memphis Tennessee 38120 —
Tennessee Oncology PLLC Nashville Tennessee 37203 —
MS Center at Evergreen Kirkland Washington 98034 —
Seattle Cancer Care Alliance Seattle Washington 98109 —
Group Health Seattle Washington 98112 —
Multicare Health System Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01900652, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 18, 2019 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01900652 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →