CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 16 enrolled
Drug / intervention
Cixutumumab +2 morebiological
Likely dose
Not stated in 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/NCT01026623
NCT01026623Phase 2Completed

Phase I/II Trial of Anti-IGF-IR Monoclonal Antibody IMC-A12 Plus mTOR Inhibitor Temsirolimus (CCI-779) in Metastatic Castration-Resistant Prostate Cancer (CRPC)

National Cancer Institute (NCI)·interventional·Posted Dec 4, 2009·Updated Jun 17, 2019

In Brief

A Phase 2 clinical trial evaluating Cixutumumab, Diagnostic Laboratory Biomarker Analysis, and 1 other intervention for Hormone-Resistant Prostate Cancer and 3 related conditions. Completed, enrolled 16 participants across 4 sites.

Detailed Summary

This phase I/II trial is studying the side effects of giving cixutumumab together with temsirolimus and to see how well it works in treating patients with metastatic prostate cancer. Monoclonal antibodies, such as cixutumumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Temsirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving cixutumumab together with temsirolimus may kill more tumor cells.

Study Details

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

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedDec 4, 2009
Enrollment StartOct 1, 2009
Primary CompletionFeb 1, 2013
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 16.6 years ago

Interventions

Cixutumumabbiological

Given IV

Diagnostic Laboratory Biomarker Analysisother

Correlative studies

Temsirolimusdrug

Given IV