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Completed Phase 1 Interventional

A Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplatin in Subjects With Cancer

ClinicalTrials.gov ID: NCT00878449

Public ClinicalTrials.gov record NCT00878449. 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 Oct 19, 2026, 11:38 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 1 Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplatin in Subjects With Cancer

Brief summary

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

This is a Phase 1 Study Evaluating the Safety of ABT-263 in Combination with Etoposide/Cisplatin in Subjects with Small Cell Lung Cancer (SCLC).

Study identification

NCT ID
NCT00878449
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
12 participants

Conditions and interventions

Conditions

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
Oct 2009 (Type not available)
Primary completion
Jul 2011 (Actual)
Completion
Jul 2011 (Actual)
Last update posted
Jun 6, 2018

2009 – 2011

United States locations

U.S. sites
7
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
Site Reference ID/Investigator# 13323 Chicago Illinois 60637 —
Site Reference ID/Investigator# 12841 Maywood Illinois 60153 —
Site Reference ID/Investigator# 12303 Baltimore Maryland 21231 —
Site Reference ID/Investigator# 12305 Boston Massachusetts 02215 —
Site Reference ID/Investigator# 20381 Boston Massachusetts 02215 —
Site Reference ID/Investigator# 43505 Detroit Michigan 48202 —
Site Reference ID/Investigator# 13322 New Brunswick New Jersey 08901 —

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 NCT00878449, 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 Jun 6, 2018 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00878449 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →