CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 47 enrolled
Drug / intervention
IMC-A12 (cixutumumab) - 10 milligrams/kilogram (mg/kg) +2 morebiological
Likely dose
IMC-A12 (cixutumumab) - 10 milligrams/kilogram (mg/kg)from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

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

Search/NCT00906373
NCT00906373Phase 2Completed

A Multicenter, Phase 2 Study Evaluating IMC-A12 in Combination With Sorafenib as First-Line Therapy for Patients With Advanced Hepatocellular Carcinoma (HCC)

Eli Lilly and Company·interventional·Posted May 21, 2009·Updated Jun 4, 2018

In Brief

A Phase 2 clinical trial evaluating IMC-A12 (cixutumumab) - 10 milligrams/kilogram (mg/kg), IMC-A12 (cixutumumab) - 20 mg/kg, and 1 other intervention for Hepatocellular Carcinoma. Completed, enrolled 47 participants across 7 sites.

Detailed Summary

To determine if IMC-A12 given in combination with Sorafenib is safe and effective for participants with advanced liver cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedMay 21, 2009
Enrollment StartMay 1, 2009
Primary CompletionOct 1, 2012
Study CompletionMay 1, 2014
TodayJul 2, 2026
Enrollment to primary: 3.4 yearsPosted 17.1 years ago

Interventions

IMC-A12 (cixutumumab) - 10 milligrams/kilogram (mg/kg)biological

intravenous infusions 10 mg/kg on Day 1 of each 3-week cycle

IMC-A12 (cixutumumab) - 20 mg/kgbiological

intravenous infusions 20 mg/kg on Day 1 of each 3-week cycle

Sorafenibdrug

400 milligrams (mg) twice per day orally