CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 23 enrolled
Drug / intervention
enzastaurindrug
Likely dose
Enzastaurin 500 mg orally once dailyAI-extracted
Key inclusion· 5
  • Prior participation in and completion of Study JCAV, JCAY, or other enzastaurin clinical pharmacology/biopharmaceutics studies
  • Advanced or metastatic cancer with no other life-prolonging therapy available
  • Measurable or detectable lesions
  • Treated, stable brain cancer allowed
Key exclusion· 5
  • Treatment with other experimental drugs within 30 days (excluding enzastaurin)
  • Pregnant or breastfeeding
  • Active untreated CNS tumors
  • Second malignancy (except adequately treated skin cancer or cancer-free >2 years)

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00309140
NCT00309140Phase 2Completed

An Open-Label Study of Oral Enzastaurin HCl in Patients With Advanced or Metastatic Malignancies

Eli Lilly and Company·interventional·Posted Mar 31, 2006·Updated Jun 26, 2020

In Brief

A Phase 2 clinical trial evaluating enzastaurin for Neoplasms and Cancer. Completed, enrolled 23 participants across 1 site.

Detailed Summary

This study will collect further basic safety data on participants with cancer treated with enzastaurin. This study is not open to the public. The purpose of the this study is to extend the clinical experience of participants who complete enzastaurin therapy per clinical pharmacology and biopharmaceutics studies conducted by Eli Lilly and Company and who may benefit from continued enzastaurin therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNeoplasms, Cancer
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 31, 2006
Enrollment StartMar 1, 2006
Primary CompletionJul 1, 2009
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 20.3 years ago

Interventions

enzastaurindrug

500 milligrams (mg), oral, daily, six 42-day cycle and subsequent cycles or until participants met study discontinuation criteria of progressive disease or unacceptable toxicity