Status:

COMPLETED

A Study of Enzastaurin in Patients With Leukemia

Lead Sponsor:

Eli Lilly and Company

Conditions:

Leukemia, Lymphocytic

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief Summary

The primary objective of this study is to see if enzastaurin affects the pGSK3 beta level in B-cell chronic lymphocytic leukemia (B-CLL) cells.

Eligibility Criteria

Inclusion

  • Patients are eligible to be included in the study only if they meet all of the following criteria:
  • Patients with B-cell CLL as diagnosed by expression of CD19, CD5, and CD23 by flow cytometry.
  • Rai Stage III or IV disease or earlier stage disease with indications for therapy per NCI Working Group criteria (Cheson et al. 1996)
  • Absolute lymphocyte count \> or = to 5,000/microliter, with a lymphocyte WBC differential of \> or = to 70%.
  • Platelet count \>20,000/microliter.
  • Adequate organ function, including the following:
  • Hepatic: bilirubin \< or = to 1.5 times the upper limit of normal (x ULN); alkaline phosphatase (ALP), aspartate transaminase (AST), and alanine transaminase (ALT) \< or = to 2.5 x ULN
  • Renal: serum creatinine \< or = to 1.5 X ULN.

Exclusion

  • Patients will be excluded from the study if they meet any of the following criteria:
  • Are unable to swallow tablets.
  • Are unable to discontinue use of carbamazepine, phenobarbital, and phenytoin.
  • Are pregnant or breastfeeding.
  • Have central nervous system (CNS) metastases (unless the patient has completed successful local therapy for CNS metastases and has been off of corticosteroids for at least 4 weeks before starting study therapy).
  • Have a serious concomitant systemic disorder (including active bacterial, fungal, or viral infection) that, in the opinion of the investigator, would compromise the patient's ability to adhere to the protocol.

Key Trial Info

Start Date :

May 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2008

Estimated Enrollment :

18 Patients enrolled

Trial Details

Trial ID

NCT00452257

Start Date

May 1 2007

End Date

September 1 2008

Last Update

March 19 2009

Active Locations (4)

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Page 1 of 1 (4 locations)

1

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Duarte, California, United States, 91010

2

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Chicago, Illinois, United States, 60612

3

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

New York, New York, United States, 10021

4

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Houston, Texas, United States, 77030