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Terminated Phase 3 Interventional Results available

A Study of ASP8273 vs. Erlotinib or Gefitinib in First-line Treatment of Patients With Stage IIIB/IV Non-small Cell Lung Cancer Tumors With EGFR Activating Mutations

ClinicalTrials.gov ID: NCT02588261

Public ClinicalTrials.gov record NCT02588261. 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 14, 2026, 7:19 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

An Open-label, Randomized Phase 3 Efficacy Study of ASP8273 vs Erlotinib or Gefitinib in First-line Treatment of Patients With Stage IIIB/IV Non-small Cell Lung Cancer Tumors With EGFR Activating Mutations

Study identification

NCT ID
NCT02588261
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Astellas Pharma Global Development, Inc.
Industry
Enrollment
530 participants

Conditions and interventions

Interventions

  • Erlotinib Drug
  • Gefitinib Drug
  • naquotinib mesilate Drug

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
Feb 10, 2016
Primary completion
Dec 20, 2017
Completion
Dec 20, 2017
Last update posted
Dec 9, 2024

2016 – 2017

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
Site US10029 Beverly Hills California 90211
Site US10025 Fountain Valley California 90806
Site US10036 La Jolla California 92093
Site US10051 Loma Linda California 92350
Site US10033 Los Angeles California 90033
Site US10031 Oxnard California 93030
Site US10052 Redondo Beach California 90277
Site US10003 Santa Monica California 90404
Site US10018 Whittier California 90603
Site US10047 Glenwood Springs Colorado 81601
Site US10013 Aventura Florida 33180
Site US10048 St. Petersburg Florida 33705
Site US10050 Atlanta Georgia 30342
Site US10042 Baton Rouge Louisiana 70809
Site US10037 Scarborough Maine 04074
Site US10034 Boston Massachusetts 02111
Site US10030 Minneapolis Minnesota 55455
Site US10027 Rochester Minnesota 55905
Site US10045 Albuquerque New Mexico 87106
Site US10012 Mount Kisco New York 10549
Site US10021 Bethlehem Pennsylvania 18015
Site US10009 Nashville Tennessee 37203
Site US10023 Nashville Tennessee 37232
Site US10011 Lacey Washington 98503
Site US10046 Milwaukee Wisconsin 53226

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 142 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02588261, 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 Dec 9, 2024 · Synced May 14, 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 NCT02588261 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →