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Study Summary
No. DM02-385:.......Leukemia; CTRC(Translational Research)......Susan O'Brien......Leukemia
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Study Summary Title
Study Summary
Number:
DM02-385
Study Title:A Phase I Multicenter, Dose-Escalation Study of IDEC - 152 (Anti-CD23 Monoclonal Antibody) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia
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Physician New Patient Referral
Name:Susan O'BrienPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:LeukemiaReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-792-7543
Contact us about clinical trials
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General Information
Disease Group:Leukemia
CTRC(Translational Research)
Supported By:IDEC Pharmaceutical Corp.
Phase of Study:Phase IReturn
Visit:
The following is a schedule of return visits for this protocol days 29, 36, 43 & 50; months 3, 6, 9, 12, 15, 18, 21, 24, 30, 36, 42, & 48 from completion of study drug.
Treatment
Agents:
idec-152Home Care:None needed
Treatment Loc:outpatient
Estimated
Length of Stay
in Houston:
4 weeks
Description/
Intervention:
Unavailable
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Study Objectives / Outcomes
Unavailable
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Study Status Information
Study Activation / Registration Date:11/15/2002
IRB Review and Approval Date:10/31/2002
Study Type:Therapeutic
Recruitment Status:Closed
Projected Accrual:70
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:Signed, written IRB-approved informed consent.


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Links
Registration Number:

Other Links:
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Results


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