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Terminated Phase 2 Interventional

Phase 2 Study to Assess the Efficacy & Safety of Gemcitabine + Nab Paclitaxel With or Without Dociparstat in Metastatic Pancreatic Cancer Patients

ClinicalTrials.gov ID: NCT01461915

Public ClinicalTrials.gov record NCT01461915. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 10:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized Phase II Open Label Study to Assess the Efficacy & Safety of Gemcitabine + Abraxane® With or Without ODSH (2-0, 3-0 Desulfated Heparin) as First Line Treatment of Metastatic Pancreatic Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, Phase 2, open label study aims to assess the efficacy and safety of gemcitabine + nab paclitaxel with or without dociparstat (ODSH) as first line treatment of metastatic pancreatic cancer. This study consists of 2 periods: a Run-in Period and a Randomized Period.

Study identification

NCT ID
NCT01461915
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Jazz Pharmaceuticals
Industry
Enrollment
60 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2011 (Type not available)
Primary completion
Dec 2012 (Actual)
Completion
Jun 2015 (Actual)
Last update posted
Jun 6, 2022

2011 – 2015

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Mayo Clinic Arizona Scottsdale Arizona 85259 —
Disney Family Cancer Center Burbank California 91505 —
Marin Cancer Care Greenbrae California 94904 —
Scripps Clinic Torrey Pines ( Green Hospital) La Jolla California 92037 —
Cleveland Clinic Florida Weston Florida 33331 —
Loyola University Medical Center/Cardinal Bernardin Cancer Center Maywood Illinois 60153 —
Indiana University Health, Goshen Center for Cancer Care Goshen Indiana 46526 —
Fesit-Weiller Cancer Center Shreveport Louisiana 71130 —
Saint Mary's Health Care Grand Rapids Michigan 49503 —
Summa Health System - Cooper Cancer Center Akron Ohio 44304 —
Thomas Jefferson University [Kimmel Cancer Center] Philadelphia Pennsylvania 19107 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
UPMC Cancer Center Pittsburgh Pennsylvania 15232 —
Medical University of South Carolina Hollings Cancer Center Charleston South Carolina 29425 —
University of Texas Medical Branch Galveston Texas 77555 —
South Texas Oncology & Hematology San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01461915, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 6, 2022 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01461915 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →