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A Study of Oral LY317615 in Relapsed or Refractory Diffuse Large B-Cell Lymphomas.

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Lilly

Status and phase

Completed
Phase 2

Conditions

Non-Hodgkin's Lymphoma

Treatments

Drug: LY317615

Study type

Interventional

Funder types

Industry

Identifiers

NCT00042666
H6Q-MC-JCAI (Other Identifier)
4849

Details and patient eligibility

About

This study will measure the effectiveness and any side effects of LY317615 in participants with diffuse large B-cell lymphoma (DLBCL: a sub-type of Non-Hodgkins Lymphoma).

Enrollment

55 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A diagnosis of recurrent or refractory DLBCL.
  • Adequate organ functions.
  • Able to swallow capsules.

Exclusion criteria

  • More than 3 prior treatments for this disease.
  • Serious heart problems.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

55 participants in 1 patient group

LY317615
Experimental group
Description:
500 milligrams (mg), oral, daily (QD), up to six (6) 28-day cycles
Treatment:
Drug: LY317615

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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