CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 279 enrolled
Drug / intervention
PEGPH20 +4 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/NCT01839487
NCT01839487Phase 2Completed

A Phase 2, Randomized, Multicenter Study of PEGPH20 (PEGylated Recombinant Human Hyaluronidase) Combined With Nab-Paclitaxel Plus Gemcitabine Compared With Nab-Paclitaxel Plus Gemcitabine in Subjects With Stage IV Previously Untreated Pancreatic Cancer

Halozyme Therapeutics·interventional·Posted Apr 25, 2013·Updated Jul 20, 2020

In Brief

A Phase 2 clinical trial evaluating PEGPH20, Nab-paclitaxel, and 3 other interventions for Metastatic Pancreatic Cancer. Completed, enrolled 279 participants across 51 sites.

Detailed Summary

This study is designed to compare the treatment effect of PEGPH20 combined with nab-paclitaxel (NAB) and gemcitabine (GEM) \[PAG\] to NAB and GEM \[AG\] in participants with Stage IV previously untreated pancreatic ductal adenocarcinoma (PDA). The study will have 2 run-in phases, one for each formulation of PEGPH20 (original and new formulations), and a Phase 2 portion. The 2 run-in phases will evaluate the safety and tolerability of the PAG treatment using the original and new succinic acid PEGPH20 formulation, respectively, compared with AG treatment. Phase 2 will have 2 stages due to a partial clinical hold that occurred from April through July 2014. The participants will be randomized in 3:1 for the run-in phases. The first stage will randomize participants in a 1:1 ratio. The second stage will randomize participants in a 2:1 ratio (PAG:AG). This is an open-label study. To minimize bias to the progression-free survival endpoint, disease progression will be based on the assessment of the Central Imaging Reader (CIR). Determination of clinical progression by the Investigator without corresponding CIR confirmation will be documented with the relevant signs and symptoms.

Study Details

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

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedApr 25, 2013
Enrollment StartMay 14, 2013
Primary CompletionMay 1, 2018
Study CompletionSep 26, 2018
TodayJul 2, 2026
Enrollment to primary: 5.0 yearsPosted 13.2 years ago

Interventions

PEGPH20drug

PEGPH20 will be administered as per the dose and schedule specified in the respective arms.

Nab-paclitaxeldrug

Nab-paclitaxel will be administered as per the dose and schedule specified in the respective arms.

Gemcitabinedrug

Gemcitabine will be administered as per the dose and schedule specified in the respective arms.

Dexamethasonedrug

Dexamethasone will be administered as per the dose and schedule specified in the respective arms.

Enoxaparindrug

Enoxaparin will be administered as per the dose and schedule specified in the respective arms.