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A Pilot Study of OSI-461 in Patients With Chronic Lymphocytic Leukemia (CLL)
NCT00073489 · View on ClinicalTrials.gov ↗
Study Summary
The objectives of this study are to evaluate the safety and efficacy of OSI-461 in CLL patients.
Conditions Studied
Interventions
- DRUG OSI-461
Study Locations (15)
Texas
- Southwest Regional Cancer Center — Austin
- Hematology Oncology Associates of South Texas — San Antonio
- Tyler Cancer Center — Tyler
Florida
- Florida Oncology Associates — Jacksonville
- Ocala Oncology Center — Ocala
Arizona
- Arizona Hematology & Oncology Associates — Phoenix
Colorado
- Rocky Mountain Cancer Centers — Aurora
Iowa
- Iowa Oncology Associates — Cedar Rapids
Missouri
- Oncology/Hematology Associates of Kansas City — Kansas City
North Carolina
- Piedmont Hem Onc Assoc, P.A. — Winston-Salem
Ohio
- Dayton Oncology/Hematology Consultants — Dayton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2001-05 |
| Est. Completion | 2003-12 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00073489
The ClinicalTrials.gov registry entry for NCT00073489 describes a study currently listed as completed. It is categorized as Phase 2, 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 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Astellas Pharma, which has 51 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Chronic Lymphocytic Leukemia appearing as the primary indexed condition, and to 1 intervention — of which OSI-461 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: NCT00073489 reports 15 study locations spanning 12 distinct geographic areas — top geographies include Texas, Florida, Arizona. 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 NCT00073489 about?
NCT00073489 is a clinical study titled "A Pilot Study of OSI-461 in Patients With Chronic Lymphocytic Leukemia (CLL)". The objectives of this study are to evaluate the safety and efficacy of OSI-461 in CLL patients.
What is the current status of trial NCT00073489?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 23 participants. The study started on 2001-05. Estimated completion is 2003-12.
What conditions does trial NCT00073489 study?
This clinical trial studies the following conditions: Chronic Lymphocytic Leukemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00073489?
The interventions under investigation include: OSI-461 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00073489?
This trial is sponsored by Astellas Pharma, which has 51 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00073489 being conducted?
This trial has 15 study locations across Arizona, Colorado, Florida, Iowa, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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