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A Phase I Study of ABT-888 in Combination With Conventional Whole Brain Radiation Therapy (WBRT) in Cancer Patients With Brain Metastases
NCT00649207 · View on ClinicalTrials.gov ↗
Study Summary
This Phase I clinical trial is studying the side effects and best dose of ABT-888 when given together with Whole Brain Radiation Therapy (WBRT) in treating patients with brain metastases.
Conditions Studied
Interventions
- DRUG ABT-888
- RADIATION Whole Brain Radiation Therapy
Study Locations (9)
Other
- Site Reference ID/Investigator# 18542 — Toronto
- Site Reference ID/Investigator# 46322 — Ponce
Georgia
- Site Reference ID/Investigator# 8334 — Atlanta
Illinois
- Site Reference ID/Investigator# 52462 — Chicago
Kansas
- Site Reference ID/Investigator# 24483 — Kansas City
Maryland
- Site Reference ID/Investigator# 7180 — Baltimore
Michigan
- Site Reference ID/Investigator# 19021 — Detroit
Pennsylvania
- Site Reference ID/Investigator# 6344 — Philadelphia
Wisconsin
- Site Reference ID/Investigator# 6653 — Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2008-03 |
| Est. Completion | 2013-03 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00649207
The ClinicalTrials.gov registry entry for NCT00649207 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 80 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 5 conditions, with Neoplasm Metastasis appearing as the primary indexed condition, and to 2 interventions — of which ABT-888 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: NCT00649207 reports 9 study locations spanning 8 distinct geographic areas — top geographies include Other, Georgia, Illinois. 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 NCT00649207 about?
NCT00649207 is a clinical study titled "A Phase I Study of ABT-888 in Combination With Conventional Whole Brain Radiation Therapy (WBRT) in Cancer Patients With Brain Metastases". This Phase I clinical trial is studying the side effects and best dose of ABT-888 when given together with Whole Brain Radiation Therapy (WBRT) in treating patients with brain metastases.
What is the current status of trial NCT00649207?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2008-03. Estimated completion is 2013-03.
What conditions does trial NCT00649207 study?
This clinical trial studies the following conditions: Neoplasm Metastasis, Central Nervous System Diseases, Brain Neoplasms, Brain Diseases, Nervous System Neoplasms. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00649207?
The interventions under investigation include: ABT-888 (DRUG), Whole Brain Radiation Therapy (RADIATION). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00649207?
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 NCT00649207 being conducted?
This trial has 9 study locations across Georgia, Illinois, Kansas, Maryland, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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