CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 46 enrolled
Drug / intervention
Erlotinib +1 moredrug
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/NCT00770263
NCT00770263Phase 1Completed

Phase I Study of Erlotinib and Temsirolimus in Resistant Solid Malignancies

Washington University School of Medicine·interventional·Posted Oct 9, 2008·Updated Jun 3, 2015

In Brief

A Phase 1 clinical trial evaluating Erlotinib and Temsirolimus for Solid Tumors. Completed, enrolled 46 participants across 1 site.

Detailed Summary

Define the maximum tolerated dose and dose limiting side-effects of temsirolimus in combination wtih erlotinib in patients with resistant solid tumors

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSolid Tumors
CountriesUnited States
CollaboratorsPfizer

Timeline

Phase 1CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 9, 2008
Enrollment StartMay 1, 2009
Primary CompletionSep 1, 2014
TodayJul 2, 2026
Enrollment to primary: 5.3 yearsPosted 17.7 years ago

Interventions

Erlotinibdrug

Temsirolimusdrug