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Terminated Phase 3 Interventional Results available

Study of Patritumab in Combination With Erlotinib in Subjects With Locally Advanced or Metastatic Non-Small-Cell Lung Cancer (NSCLC). (HER3-Lung)

ClinicalTrials.gov ID: NCT02134015

Public ClinicalTrials.gov record NCT02134015. 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 May 17, 2026, 6:06 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

Phase 3, Randomized, Placebo-Controlled, Double-Blind, Multi-Center, Two-Part Study of Patritumab (U3-1287) In Combination With Erlotinib in EGFR Wild-type Subjects With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) Who Have Progressed on at Least One Prior Systemic Therapy

Study identification

NCT ID
NCT02134015
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Daiichi Sankyo
Industry
Enrollment
145 participants

Conditions and interventions

Interventions

  • Erlotinib Drug
  • Patritumab Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
20 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
Feb 28, 2014
Primary completion
Nov 10, 2016
Completion
Nov 10, 2016
Last update posted
Jan 22, 2018

2014 – 2016

United States locations

U.S. sites
26
U.S. states
17
U.S. cities
26
Facility City State ZIP Site status
Not listed Glendale Arizona
Not listed Duarte California
Not listed La Verne California
Not listed Los Angeles California 43210
Not listed San Francisco California
Not listed Port Saint Lucie Florida
Not listed Tampa Florida
Not listed Chicago Illinois
Not listed Maywood Illinois
Not listed Goshen Indiana 46526
Not listed Louisville Kentucky
Not listed Grand Rapids Michigan
Not listed Saint Cloud Minnesota
Not listed St Louis Missouri
Not listed Las Vegas Nevada
Not listed Columbus Ohio
Not listed Bend Oregon
Not listed Portland Oregon
Not listed Redmond Oregon 97756
Not listed Chattanooga Tennessee
Not listed Knoxville Tennessee
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed Salt Lake City Utah
Not listed Arlington Virginia
Not listed Seattle Washington

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 72 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02134015, 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 Jan 22, 2018 · Synced May 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02134015 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →