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Completed Phase 2 Interventional Results available

A Study Of Dacomitinib (PF-00299804) In Patients With Advanced Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT01858389

Public ClinicalTrials.gov record NCT01858389. 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 5, 2026, 5:34 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 2 Open Label Trial Of Oral Intermittent Dacomitinib In Patients With Advanced Nsclc

Brief summary

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

This is a Phase 2 study of oral dacomitinib given every 12 hours over days 1-4 of each two-week cycle to patients with Non-small cell lung cancer. The study includes two groups of patients, those whose tumor has a documented T790M mutation, and those without this mutation. All patients will receive repeated cycles of dacomitinib until disease progression, occurrence of unacceptable toxicity, or other withdrawal criteria are met.

Study identification

NCT ID
NCT01858389
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
41 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
Jun 30, 2013
Primary completion
Aug 31, 2015
Completion
Aug 31, 2015
Last update posted
Jul 17, 2017

2013 – 2015

United States locations

U.S. sites
12
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
Tower Hematology Oncology Medical Group Beverly Hills California 90211
Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute Los Angeles California 90048
Georgetown University Hospital-Lombardi Comprehensive Cancer Center Washington D.C. District of Columbia 20007
Georgetown University Medical Center Department of Pharmacy, Research Washington D.C. District of Columbia 20007
Memorial Sloan-Kettering Cancer Center-Rockefeller Outpatient Pavilion New York New York 10022
Investigational Drug Service, Hillman Cancer Center Pittsburgh Pennsylvania 15232
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15232
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232
UT Southwestern Medical Center-Simmons Cancer Center Pharmacy Dallas Texas 75390-9015
UT Southwestern Medical Center Dallas Texas 75390
UT Southwestern University Hospital - William P. Clements, Jr. Dallas Texas 75390
UT Southwestern University Hospital - Zale Lipshy Dallas Texas 75390

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01858389, 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 Jul 17, 2017 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01858389 live on ClinicalTrials.gov.

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