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Completed Phase 3 Interventional

Masitinib in Combination With Gemcitabine for Treatment of Patients With Advanced/Metastatic Pancreatic Cancer

ClinicalTrials.gov ID: NCT00789633

Public ClinicalTrials.gov record NCT00789633. 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 Sep 6, 2026, 12:36 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 Prospective, Multicenter, Randomized, Double-blind, Placebo-controlled, 2-parallel Group, Phase III Study to Compare Efficacy and Safety of Masitinib 9 mg/kg/Day in Combination With Gemcitabine Compared to Placebo in Combination With Gemcitabine in Treatment of Patients With Advanced/Metastatic Pancreatic Cancer

Brief summary

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

The objective of this study is to compare the efficacy and safety of masitinib in combination with gemcitabine to placebo in combination with gemcitabine in patients with advanced/metastatic pancreatic cancer.

Study identification

NCT ID
NCT00789633
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AB Science
Industry
Enrollment
353 participants

Conditions and interventions

Interventions

Drug

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 24, 2008
Primary completion
Dec 22, 2011
Completion
Aug 30, 2012
Last update posted
Dec 16, 2018

2008 – 2012

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Eastern Connecticut Hematology and Oncology (ECHO) Norwich Connecticut 06360
MD Anderson Orlando Florida 32806
The Emory Clinic Atlanta Georgia 30322
Decatur Memorial Hospital Decatur Illinois 62526
Medical & Surgical Specialists Galesburg Illinois 61401
Berkshire Hematology Oncology Pittsfield Massachusetts 01201
Henry Ford Health System Detroit Michigan 48202
Metro MN CCOP Saint Louis Park Minnesota 55416
Saint Luke's Cancer Institute Kansas City Missouri 64111
The Valley Hospital Paramus New Jersey 07652
Southeastern Medical Oncology Center Goldsboro North Carolina 27534
Oregon Health & Science University Portland Oregon 97239

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 56 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00789633, 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 Dec 16, 2018 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00789633 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →