CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 60 enrolled
Drug / intervention
erlotinib hydrochloride +2 moredrug
Likely dose
erlotinib hydrochloride 50 mgfrom 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/NCT00425386
NCT00425386Phase 2Completed

A Dose Escalation Phase II Study of Sunitinib Plus Erlotinib in Advanced Renal Carcinoma

OHSU Knight Cancer Institute·interventional·Posted Jan 23, 2007·Updated May 3, 2017

In Brief

A Phase 2 clinical trial evaluating erlotinib hydrochloride, sunitinib malate, and 1 other intervention for Kidney Cancer. Completed, enrolled 60 participants across 4 sites.

Detailed Summary

RATIONALE: Sunitinib and erlotinib may stop the growth of tumor cell by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Giving sunitinib together with erlotinib may kill more tumor cells. PURPOSE: This phase II trial is studying the best dose of erlotinib when given together with sunitinib and to see how well they work in treating patients with unresectable or metastatic kidney cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsKidney Cancer
CountriesUnited States

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJan 23, 2007
Enrollment StartAug 1, 2006
Primary CompletionAug 1, 2010
Study CompletionMar 1, 2014
TodayJul 2, 2026
Enrollment to primary: 4 yearsPosted 19.4 years ago

Interventions

erlotinib hydrochloridedrug

Dose Level 0 = 50 mg/day, continuous daily; 0.5= 75 mg/day, continuous daily; 1. 100 mg/day, continuous daily; 1.5= 125 mg/day, continuous daily; 2. 150 mg/day, continuous daily

sunitinib malatedrug

Will be administered at 50 mg daily, 4 weeks on, 2 weeks off

biopsyprocedure

Paraffin block (or unstained slides) of the primary tumor and/or metastatic lesions (as available) and a plasma sample for future correlative studies will be collected. A paraffin block (or at least 10 unstained slides, each of 10 micromillimeter thickness) from the original paraffin-embedded biopsy material taken at the diagnosis will be stored at 4 degrees Celsius.