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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 Sep 7, 2026, 10:22 AM 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
Jul 31, 2013
Primary completion
Jan 31, 2015
Completion
Feb 29, 2016
Last update posted
Sep 17, 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 17, 2019 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01900652 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →