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Completed Phase 1Phase 2 Interventional

STA-4783 in Combination With Paclitaxel and Carboplatin for the Treatment of Chemotherapy Naive Patients With Stage IIIB/IV Non Small Cell Lung Cancer (NSCLC)

ClinicalTrials.gov ID: NCT00088088

Public ClinicalTrials.gov record NCT00088088. 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 29, 2026, 9:23 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

A Phase I/II Trial of STA-4783 in Combination With Paclitaxel and Carboplatin for the Treatment of Chemotherapy Naive Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer (NSCLC)

Brief summary

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

This study is for patients who have Stage IIIb or Stage IV NSCLC and have never had chemotherapy before for their disease. The first phase of the study recently completed and for the second phase of the study patients are randomly assigned to receive either paclitaxel and carboplatin or paclitaxel and carboplatin and study drug (STA 4783). Treatment will be every 3 weeks for 6 cycles.

Study identification

NCT ID
NCT00088088
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Synta Pharmaceuticals Corp.
Industry
Enrollment
86 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
Feb 29, 2004
Primary completion
Not listed
Completion
Feb 28, 2005
Last update posted
Dec 3, 2008

2004 – 2005

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
NEA Clinic Jonesboro Arkansas 72401 —
Wilshire Oncology Medical Group Pomona California 91767 —
St. Francis Memorial Hospital San Francisco California — —
Cancer Institute Medical Group Santa Monica California 90404 —
Kaiser Permanete Vallejo California — —
Oncology Associates of Bridgeport Trumball Connecticut 06611 —
ACORN Miami Florida — —
Oncology Hematology Consultants Sarasota Florida 34236 —
University of Chicago Chicago Illinois 60637 —
The Cancer Institute at Alexian Brothers Elk Grove Village Illinois 60007 —
Ingalls Hospital Harvey Illinois 60426 —
Overton Brooks, VAMC Shreveport Louisiana 71101 —
LSUHSC - Shreveport Feist Weiller Cancer Center Shreveport Louisiana 71130 —
Maryland Hematology and Oncology Associates Baltimore Maryland 21236 —
The Duluth Clinic Duluth Minnesota 55805 —
The West Clinic Memphis Tennessee 38120 —
The Sarah Cannon Research Center Nashville Tennessee 37203 —
Presbyterian Hospital Dallas Texas 75231 —
Multicare Health System Tacoma Washington 98405 —

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 NCT00088088, 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 3, 2008 · Synced Sep 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00088088 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →