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NCT00546793 · ClinicalTrials.gov registry record · Phase 1
Ph I/II Study of Subcutaneously Administered Veltuzumab (hA20) in NHL and CLL
A Phase 1 study, sponsored by Gilead Sciences.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
NCT00546793: Completed Phase 1 study, sponsored by Gilead Sciences.
NCT00546793 is a Phase 1 study that has completed, run by Gilead Sciences. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00546793, a Phase 1 study, has completed, sponsored by Gilead Sciences.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if a subcutaneous (SC) dosing schedule of veltuzumab can be established in NHL or CLL patients and to confirm the safety and efficacy of veltuzumab that was previously established when administered intravenously.
Primary Outcome
safety will be assessed by monitoring lab results and adverse events, which will be assessed every 3 months for up to 2 years.
Interventions
- BIOLOGICAL veltuzumab
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2008-01 |
| Est. Completion | 2013-03 |
| Phase | Phase 1 |
What the finished NCT00546793 record still lists
NCT00546793 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).
The record links to 0 conditions, and to 1 intervention - of which veltuzumab is the first listed.
NCT00546793 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00546793 about?
NCT00546793 is a clinical study titled "Ph I/II Study of Subcutaneously Administered Veltuzumab (hA20) in NHL and CLL". The purpose of this study is to determine if a subcutaneous (SC) dosing schedule of veltuzumab can be established in NHL or CLL patients and to confirm the safety and efficacy of veltuzumab that was previously established when administered intravenously.
What is the current status of trial NCT00546793?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2008-01. Estimated completion is 2013-03.
What interventions are being tested in trial NCT00546793?
The interventions under investigation include: veltuzumab (BIOLOGICAL).
Who is sponsoring clinical trial NCT00546793?
This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00546793's enrollment target sits among peer trials
32 1296th of 2000 higher than 679 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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