Status:

COMPLETED

Oral Enzastaurin in Participants With Relapsed Mantle Cell Lymphoma

Lead Sponsor:

Eli Lilly and Company

Conditions:

Mantle-Cell Lymphoma

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

The purposes of this study are to determine the safety of oral enzastaurin and any side effects that might be associated with it and whether enzastaurin can help participants with mantle cell lymphoma...

Eligibility Criteria

Inclusion

  • Mantle cell lymphoma
  • Previous treatment for mantle cell lymphoma
  • Previously relapsed mantle cell lymphoma with no more than 4 chemotherapy regimens.
  • Have discontinued all previous therapies for cancer, except corticosteroids up to 25 milligrams per day (mg/day)
  • Adequate organ function

Exclusion

  • Inability to swallow tablets
  • Must not have significant heart problems

Key Trial Info

Start Date :

March 1 2004

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2008

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT00088205

Start Date

March 1 2004

End Date

May 1 2008

Last Update

July 1 2020

Active Locations (17)

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Page 1 of 5 (17 locations)

1

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician

Woolloongabba, Queensland, Australia

2

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician

Parkville, Victoria, Australia

3

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician

Prahran, Victoria, Australia

4

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician

Wodonga, Victoria, Australia