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Terminated Phase 2 Interventional Results available

Carboplatin and Paclitaxel With or Without Vorinostat in Treating Patients With Advanced Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT01413750

Public ClinicalTrials.gov record NCT01413750. 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 26, 2026, 6:16 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

Phase II Randomized Study of Vorinostat or Placebo in Combination With Carboplatin and Paclitaxel for Patients With Advanced Non-small Cell Lung Cancer

Brief summary

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

Drugs used in chemotherapy, such as carboplatin and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether giving carboplatin and paclitaxel together is more effective with or without vorinostat in treating non-small cell lung cancer.

Study identification

NCT ID
NCT01413750
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
23 participants

Conditions and interventions

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
Nov 7, 2010
Primary completion
Apr 13, 2013
Completion
Apr 13, 2013
Last update posted
Nov 11, 2024

2010 – 2013

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
City of Hope Comprehensive Cancer Center Duarte California 91010 —
USC / Norris Comprehensive Cancer Center Los Angeles California 90033 —
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
Moffitt Cancer Center Tampa Florida 33612 —
Emory University Hospital/Winship Cancer Institute Atlanta Georgia 30322 —
Illinois CancerCare-Peoria Peoria Illinois 61615 —
Southern Illinois University School of Medicine Springfield Illinois 62702 —
Mercy Hospital Saint Louis St Louis Missouri 63141 —
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599 —
Penn State Milton S Hershey Medical Center Hershey Pennsylvania 17033-0850 —
University of Pittsburgh Cancer Institute (UPCI) Pittsburgh Pennsylvania 15232 —
Vanderbilt University/Ingram Cancer Center Nashville Tennessee 37232 —
Virginia Commonwealth University/Massey Cancer Center Richmond Virginia 23298 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01413750, 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 Nov 11, 2024 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01413750 live on ClinicalTrials.gov.

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