At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 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.
Phase II Trial of Weekly Erlotinib Dosing to Reduce Duodenal Polyp Burden Associated With Familial Adenomatous Polyposis
In Brief
A Phase 2 clinical trial evaluating Erlotinib and Erlotinib Hydrochloride for Attenuated Familial Adenomatous Polyposis and Familial Adenomatous Polyposis. Completed, enrolled 46 participants across 8 sites in 2 countries.
Detailed Summary
This phase II trial studies the side effects of erlotinib hydrochloride and how well it works in reducing duodenal polyp burden in patients with familial adenomatous polyposis at risk of developing colon cancer. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPuerto Rico, United States
Collaborators--
Timeline
Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedNov 2016
Enrollment StartOct 2017
Primary CompletionFeb 2020
Study CompletionSep 2021
TodayJul 2026
First PostedNov 11, 2016
Enrollment StartOct 27, 2017
Primary CompletionFeb 23, 2020
Study CompletionSep 27, 2021
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 9.6 years ago
Interventions
Erlotinibdrug
Given PO
Erlotinib Hydrochloridedrug
Given PO