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A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or Other Non-Hematological Malignancies
NCT00445198 · View on ClinicalTrials.gov ↗
Study Summary
The Phase 1 portion of the study will evaluate the pharmacokinetic profile and safety of ABT-263 with the objective of defining the dose limiting toxicity and maximum tolerated dose. (This portion of the study is complete). The Phase 2a portion of the study will evaluate ABT-263 at the defined recommended Phase 2 dose to obtain additional safety information and a preliminary assessment of efficacy.
Conditions Studied
Interventions
- DRUG ABT-263
Study Locations (18)
Other
- Site Reference ID/Investigator# 7493 — Edmonton
- Site Reference ID/Investigator# 7635 — Ottawa
- Site Reference ID/Investigator# 18541 — Leicester
- Site Reference ID/Investigator# 2622 — Manchester
Arizona
- Site Reference ID/Investigator# 13605 — Peoria
- Site Reference ID/Investigator# 5261 — Phoenix
California
- Site Reference ID/Investigator# 11942 — Los Angeles
- Site Reference ID/Investigator# 4718 — Sacramento
Maryland
- Site Reference ID/Investigator# 2625 — Baltimore
- Site Reference ID/Investigator# 12343 — Bethesda
Massachusetts
- Site Reference ID/Investigator# 11941 — Boston
- Site Reference ID/Investigator# 2626 — Boston
Colorado
- Site Reference ID/Investigator# 3755 — Aurora
Georgia
- Site Reference ID/Investigator# 8324 — Atlanta
Illinois
- Site Reference ID/Investigator# 2623 — Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 86 participants |
| Start Date | 2007-04 |
| Est. Completion | 2010-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00445198
The ClinicalTrials.gov registry entry for NCT00445198 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 86 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie (prior sponsor, Abbott), which has 16 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Small Cell Lung Cancer appearing as the primary indexed condition, and to 1 intervention — of which ABT-263 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00445198 reports 18 study locations spanning 11 distinct geographic areas — top geographies include Other, Arizona, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00445198 about?
NCT00445198 is a clinical study titled "A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or Other Non-Hematological Malignancies". The Phase 1 portion of the study will evaluate the pharmacokinetic profile and safety of ABT-263 with the objective of defining the dose limiting toxicity and maximum tolerated dose. (This portion of the study is complete). The Phase 2a portion of the study will evaluate ABT-263 at the defined recom...
What is the current status of trial NCT00445198?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 86 participants. The study started on 2007-04. Estimated completion is 2010-12.
What conditions does trial NCT00445198 study?
This clinical trial studies the following conditions: Small Cell Lung Cancer, Small Cell Lung Carcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00445198?
The interventions under investigation include: ABT-263 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00445198?
This trial is sponsored by AbbVie (prior sponsor, Abbott), which has 16 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00445198 being conducted?
This trial has 18 study locations across Arizona, California, Colorado, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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