CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 42 enrolled
Drug / intervention
Gemcitabine +2 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/NCT01828034
NCT01828034Phase 2Completed

A Phase I/II Study of First Line Gemcitabine, Cisplatin and MEK162 in Advanced Biliary Tract Carcinoma

Memorial Sloan Kettering Cancer Center·interventional·Posted Apr 10, 2013·Updated Nov 17, 2020

In Brief

A Phase 2 clinical trial evaluating Gemcitabine, Cisplatin, and 1 other intervention for Advanced Biliary Tract Carcinoma. Completed, enrolled 42 participants across 1 site.

Detailed Summary

The purpose of this study is to test an investigational combination of drugs for bile duct or gallbladder cancers. Gemcitabine and cisplatin are two forms of chemotherapy commonly used in combination to treat bile duct and gallbladder cancers. The investigators are looking to improve treatment results. They will attempt to do so by adding the drug MEK162 to the treatment plan. MEK162 acts by blocking a protein called MEK 1/2 which helps cancer cells grow and divide. This study will help answer the question of whether MEK162 is a helpful drug in patients with bile duct or gallbladder cancers when given with gemcitabine and cisplatin.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsArray BioPharma

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedApr 10, 2013
Enrollment StartApr 1, 2013
Primary CompletionMay 30, 2019
TodayJul 2, 2026
Enrollment to primary: 6.2 yearsPosted 13.2 years ago

Interventions

Gemcitabinedrug

Cisplatindrug

MEK162drug