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Study of the Safety and Tolerability of PCI-32765 in Patients With Recurrent B Cell Lymphoma
NCT00849654 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to establish the safety and optimal dose of orally administered PCI-32765 in patients with recurrent B cell lymphoma.
Conditions Studied
Interventions
- DRUG PCI-32765
Study Locations (9)
Washington
- Northwest Cancer Specialists, Vancouver Cancer Center — Vancouver
- Yakima Valley Memorial Hospital/North Star Lodge Cancer Ctr — Yakima
California
- Stanford University School of Medicine — Palo Alto
Illinois
- University of Chicago — Chicago
Maryland
- National Cancer Institute — Bethesda
New York
- New York Prebyterian Hospital Cornell Medical Center — New York
Oregon
- Willamette Valley Cancer Institute/Research Ctr — Eugene
Texas
- University of Texas, MD Anderson — Houston
Vermont
- University of Vermont College of Medicine — Burlington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2009-02 |
| Est. Completion | 2012-07 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00849654
The ClinicalTrials.gov registry entry for NCT00849654 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 66 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pharmacyclics, which has 13 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 B-Cell Lymphoma appearing as the primary indexed condition, and to 1 intervention — of which PCI-32765 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: NCT00849654 reports 9 study locations spanning 8 distinct geographic areas — top geographies include Washington, California, 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 NCT00849654 about?
NCT00849654 is a clinical study titled "Study of the Safety and Tolerability of PCI-32765 in Patients With Recurrent B Cell Lymphoma". The purpose of this study is to establish the safety and optimal dose of orally administered PCI-32765 in patients with recurrent B cell lymphoma.
What is the current status of trial NCT00849654?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 66 participants. The study started on 2009-02. Estimated completion is 2012-07.
What conditions does trial NCT00849654 study?
This clinical trial studies the following conditions: B-Cell Lymphoma, B-Cell 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 NCT00849654?
The interventions under investigation include: PCI-32765 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00849654?
This trial is sponsored by Pharmacyclics, which has 13 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00849654 being conducted?
This trial has 9 study locations across California, Illinois, Maryland, New York, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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