ClinicalTrials.gov record
Completed Phase 1Phase 2 Interventional

A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or Other Non-Hematological Malignancies

ClinicalTrials.gov ID: NCT00445198

Public ClinicalTrials.gov record NCT00445198. 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 May 6, 2026, 8:27 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 1/2a Study Evaluating the Safety, Pharmacokinetics, and Efficacy of ABT-263 in Subjects With Small Cell Lung Cancer or Other Non-Hematological Malignancies

Study identification

NCT ID
NCT00445198
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
86 participants

Conditions and interventions

Interventions

  • ABT-263 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
Mar 31, 2007
Primary completion
Nov 30, 2010
Completion
Nov 30, 2010
Last update posted
Jun 5, 2018

2007 – 2010

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Site Reference ID/Investigator# 13605 Peoria Arizona 85381
Site Reference ID/Investigator# 5261 Phoenix Arizona 85013
Site Reference ID/Investigator# 11942 Los Angeles California 90095-7187
Site Reference ID/Investigator# 4718 Sacramento California 95817
Site Reference ID/Investigator# 3755 Aurora Colorado 80045-0510
Site Reference ID/Investigator# 8324 Atlanta Georgia 30322
Site Reference ID/Investigator# 2623 Chicago Illinois 60612
Site Reference ID/Investigator# 2625 Baltimore Maryland 21231-1000
Site Reference ID/Investigator# 12343 Bethesda Maryland 20892
Site Reference ID/Investigator# 11941 Boston Massachusetts 02215
Site Reference ID/Investigator# 2626 Boston Massachusetts 02215
Site Reference ID/Investigator# 4934 Charlotte North Carolina 28204
Site Reference ID/Investigator# 2624 Nashville Tennessee 37203
Site Reference ID/Investigator# 6650 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00445198, 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 5, 2018 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00445198 live on ClinicalTrials.gov.

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