CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 30 enrolled
Drug / intervention
Cisplatin +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/NCT03579771
NCT03579771Phase 2Completed

A Single-Arm Feasibility Study of Gemcitabine, Cisplatin, and Nab-Paclitaxel as Neoadjuvant Therapy for Resectable Oncologically High-Risk Intrahepatic Cholangiocarcinoma

Emory University·interventional·Posted Jul 9, 2018·Updated Aug 15, 2025

In Brief

A Phase 2 clinical trial evaluating Cisplatin, Gemcitabine, and 1 other intervention for Resectable Cholangiocarcinoma and 5 related conditions. Completed, enrolled 30 participants across 7 sites.

Detailed Summary

This phase II trial studies how well gemcitabine, cisplatin, and nab-paclitaxel work before surgery in treating participants with high-risk bile duct cancer in the liver (intrahepatic cholangiocarcinoma). Drugs used in chemotherapy, such as nab-paclitaxel, cisplatin, and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving combination chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

Study Details

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedJul 9, 2018
Enrollment StartSep 26, 2018
Primary CompletionSep 16, 2023
TodayJul 2, 2026
Enrollment to primary: 5.0 yearsPosted 8.0 years ago

Interventions

Cisplatindrug

Given IV

Gemcitabinedrug

Given IV

Nab-paclitaxeldrug

Given IV