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NCT00949988 · ClinicalTrials.gov registry record · Phase 1

A Study of Dasatinib and Rituximab for Relapsed/Refractory Chronic Lymphocytic Leukemia

A Phase 1 study, sponsored by University of California, San Diego.

Terminated
Registry status
Phase 1
Development phase
3
Enrollment target

NCT00949988: Clinical Trial Phase 1 study, sponsored by University of California, San Diego.

NCT00949988 is a Phase 1 study that was terminated before completion, run by University of California, San Diego. The registered enrollment target is 3 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00949988, a Phase 1 study, was terminated before completion, sponsored by University of California, San Diego.

TERMINATED
Registry status
Phase 1
Development phase
3 participants
Enrollment target

Study Summary

This is an open-label phase I/II study that will investigate the combination of dasatinib and rituximab therapy in patients with relapsed/refractory CLL. In phase I, eligible subjects will take either 100 mg or 140 mg of dasatinib daily along with rituximab on day 1 of each cycle for 6 cycles. In phase II, eligible subjects will all receive the same dose of dasatinib, as established in the phase I portion, along with rituximab on day 1 of each cycle for 6 cycles. The investigators hypothesize that the combination of dasatinib and rituximab will demonstrate efficacy in the treatment of patients with relapsed/refractory CLL.

Interventions

  • DRUG Dasatinib and Rituximab

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2009-05
Est. Completion 2012-04
Phase Phase 1
University of California, San Diego

775 total trials

Why NCT00949988 stopped before completion

NCT00949988 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which Dasatinib and Rituximab is the first listed.

NCT00949988 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00949988 about?

NCT00949988 is a clinical study titled "A Study of Dasatinib and Rituximab for Relapsed/Refractory Chronic Lymphocytic Leukemia". This is an open-label phase I/II study that will investigate the combination of dasatinib and rituximab therapy in patients with relapsed/refractory CLL. In phase I, eligible subjects will take either 100 mg or 140 mg of dasatinib daily along with rituximab on day 1 of each cycle for 6 cycles. In ph...

What is the current status of trial NCT00949988?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 3 participants. The study started on 2009-05. Estimated completion is 2012-04.

What interventions are being tested in trial NCT00949988?

The interventions under investigation include: Dasatinib and Rituximab (DRUG).

Who is sponsoring clinical trial NCT00949988?

This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00949988's enrollment target sits among peer trials

3 1999th of 2000 higher than 1 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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Source: ClinicalTrials.gov NCT00949988, the US trial registry maintained by the National Library of Medicine. NCT00949988 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.