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A Study of LY317615 in Patients With Brain Tumors

A Phase II Trial of LY317615 in Patients With Recurrent High-Grade Gliomas

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00190723
Enrollment
120
Registered
2005-09-19
Start date
2002-10-31
Completion date
2006-12-31
Last updated
2007-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Glioma

Brief summary

1. The safety of LY317615 and any side effects that might be associated with the drug. 2. Whether LY317615, can help patients with brain tumors.

Interventions

DRUGEnzastaurin

Sponsors

Eli Lilly and Company
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* You must be at least 18 years old * You must have been diagnosed with a recurrent brain tumor by MRI or CT scan * You must be able to swallow the LY317615 tablets

Exclusion criteria

* You are a woman who is pregnant or breastfeeding * In view of your doctor, you have significant heart, liver, kidney, or psychiatric disease

Design outcomes

Primary

MeasureTime frame
To establish data regarding the anti-tumor activity of LY317615 in patients with recurrent high-grade gliomas.

Secondary

MeasureTime frame
To obtain preliminary information regarding the spectrum of toxicities of LY317615 administered to patients with recurrent high-grade gliomas

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026