Safety Study of XL844 in Subjects With Chronic Lymphocytic Leukemia

NCT00234481 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL

Last updated 2008-06-04

No results posted yet for this study

Summary

The purpose of this study is to assess the safety and tolerability of different doses of XL844 when given orally to adults with recurrent or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma.

Conditions

Interventions

DRUG

XL844

Sponsors & Collaborators

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00234481 on ClinicalTrials.gov