CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 42 enrolled
Drug / intervention
NabCG (nab-Paclitaxel + Cisplatin + Gemcitabine)drug
Likely dose
NabCG (nab-Paclitaxel + Cisplatin + Gemcitabine) 25mg/m2from 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/NCT03915444
NCT03915444Phase 2Completed

A Phase II Trial of Nab-Paclitaxel Plus Cisplatin Plus Gemcitabine in Patients With Previously Untreated Metastatic Pancreatic Ductal Adenocarcinoma

HonorHealth Research Institute·interventional·Posted Apr 16, 2019·Updated Apr 23, 2026

In Brief

A Phase 2 clinical trial evaluating NabCG (nab-Paclitaxel + Cisplatin + Gemcitabine) for Pancreatic Ductal Adenocarcinoma. Completed, enrolled 42 participants across 4 sites.

Detailed Summary

This is a phase II open-label study evaluating the efficacy and safety of nab-paclitaxel cisplatin, and gemcitabine in patients with metastatic pancreatic ductal adenocarcinoma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsCelgene

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedApr 16, 2019
Enrollment StartJul 15, 2019
Primary CompletionMay 13, 2022
Study CompletionJan 23, 2023
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 7.2 years ago

Interventions

NabCG (nab-Paclitaxel + Cisplatin + Gemcitabine)drug

Cisplatin 25mg/m2 in 500 mL of NS over 60 minute IV infusion on days 1 and 8 repeated every 21 days. Gemcitabine 1000mg/m2 in 500 mL\* over 30 minute IV infusion on days 1 and 8 repeated every 21 days. Post cisplatin hydration: IV fluids up to 1000 mL (with additives as clinically indicated) IV given as infusion on days cisplatin is administered on days 1 and 8 repeated every 21 days.