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Completed Phase 2 Interventional

A Study of BIND-014 (Docetaxel Nanoparticles for Injectable Suspension) as Second-line Therapy for Patients With KRAS Positive or Squamous Cell Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT02283320

Public ClinicalTrials.gov record NCT02283320. 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 Jul 24, 2026, 9:48 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

An Open Label, Multicenter, Phase 2 Study to Determine the Safety and Efficacy of BIND-014 (Docetaxel Nanoparticles for Injectable Suspension) as a Second-Line Therapy for Patients With KRAS Mutation Positive or Squamous Cell Non-Small Cell Lung Cancer

Study identification

NCT ID
NCT02283320
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
BIND Therapeutics
Industry
Enrollment
69 participants

Conditions and interventions

Interventions

  • BIND-014 (Docetaxel Nanoparticles for Injectable Suspension) 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
Aug 31, 2014
Primary completion
Mar 31, 2016
Completion
Mar 31, 2016
Last update posted
Apr 17, 2016

2014 – 2016

United States locations

U.S. sites
22
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
Investigative Site: #51 Chandler Arizona 85224
Investigative Site: #30 Goodyear Arizona 85338
Investigative Site: #44 Phoenix Arizona 85016
Investigative Site: #41 Sedona Arizona 86336
Investigative Site: #58 Duarte California 91010
Investigative Site: #47 La Jolla California 92093
Investigative Site: #32 Los Angeles California 90048
Investigative Site: #50 San Francisco California 94115
Investigative Site: #46 Fort Meyers Florida 33916
Investigative Site: #53 Newnan Georgia 30265
Investigative Site: #56 Savannah Georgia 31405
Investigative Site: #35 Zion Illinois 60099
Investigative Site: #36 Las Vegas Nevada 89119
Investigative Site: #60 Portland Oregon 97239
Investigative Site: #34 Pittsburgh Pennsylvania 15232
Investigative Site: # 59 Pittsburgh Pennsylvania 15240
Investigative Site: #39 Amarillo Texas 79106
Investigative Site: #42 Dallas Texas 75231
Investigative Site: 38 Dallas Texas 75237
Investigative Site: #40 Blacksburg Virginia 24060
Investigative Site: #45 Vancouver Washington 98684
Investigative Site: #37 Yakima Washington 98902

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02283320, 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 Apr 17, 2016 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02283320 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →