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Completed Phase 2 Interventional Results available

Study of Safety and Tolerability of PCI-27483 in Patients With Pancreatic Cancer Patients Receiving Treatment With Gemcitabine

ClinicalTrials.gov ID: NCT01020006

Public ClinicalTrials.gov record NCT01020006. 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 21, 2026, 12:11 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

Phase II Study of Coagulation Factor VIIa Inhibitor PCI-27483 in Pancreatic Cancer Patients Receiving Treatment With Gemcitabine

Brief summary

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

The purpose of this study is to evaluate the safety and tolerability of selected dose 1.2mg/kg BID dosage administered subcutaneously (SC) administered PCI-27483 to metastatic or locally advanced pancreatic cancer patients receiving concurrent therapy with intravenously administered gemcitabine for 12 weeks.

Study identification

NCT ID
NCT01020006
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pharmacyclics LLC.
Industry
Enrollment
42 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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 2009 (Type not available)
Primary completion
Aug 2012 (Actual)
Completion
Not listed
Last update posted
Apr 24, 2014

Started 2009

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
TGen Clinical Reserch Services at Scottsdale Healthcare Scottsdale Arizona 85258 —
Pacific Cancer Medical Center Anaheim California 92081 —
Space Coast Medical Associates Titusville Florida 32796 —
Investigative Clinical Research of Indiana Indianapolis Indiana 46260 —
Kenthucky Cancer Clinic Hazard Kentucky 41701 —
Park Nicollet Institute Saint Louis Park Minnesota 55426 —
Beth Israel Cancer Center New York New York 10003 —
Columbia University New York New York 10032 —
University of Rochester Rochester New York 14642 —
Summa Health System Akron Ohio 44304 —
Gabrail Cancer Center Research Canton Ohio 44718 —
Gettysburg Cancer Center Gettysburg Pennsylvania 17325 —
Charleston Hematology Oncology Associates Charleston South Carolina 29414 —
South Carolina Cancer Specialists, PA Hilton Head South Carolina 29926 —
Associates in Oncology and Hematology Chattanooga Tennessee 37404 —
Sammons Cancer Center Dallas Texas 75246 —
University of Vermont/Vermont Cancer Center Burlington Vermont 05401 —

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 NCT01020006, 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 Apr 24, 2014 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01020006 live on ClinicalTrials.gov.

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