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Spots Global Cancer Trial Database for A Study of Nab-Paclitaxel and Gemcitabine With or Without Olaratumab (LY3012207) in Participants With Metastatic Pancreatic Cancer

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Trial Identification

Brief Title: A Study of Nab-Paclitaxel and Gemcitabine With or Without Olaratumab (LY3012207) in Participants With Metastatic Pancreatic Cancer

Official Title: A Phase 1b (Open-Label) / Phase 2 (Randomized, Double-Blinded) Study Evaluating Nab-Paclitaxel and Gemcitabine With or Without Olaratumab in the Treatment of First-Line Metastatic Pancreatic Cancer

Study ID: NCT03086369

Study Description

Brief Summary: The purpose of this study is to determine the safety and efficacy of nab-paclitaxel and gemcitabine with or without olaratumab in the treatment of first-line metastatic pancreatic cancer.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

TGen Clinical Research Services at Scottsdale Healthcare, Scottsdale, Arizona, United States

University of Arizona Cancer Center, Tucson, Arizona, United States

Highlands Oncology Group, Fayetteville, Arkansas, United States

Comprehensive Blood and Cancer Center, Bakersfield, California, United States

St Jude Medical Center, Fullerton, California, United States

TRIO - Translational Research in Oncology-US, Inc., Los Angeles, California, United States

UCLA Medical Center, Los Angeles, California, United States

Cancer Center of Santa Barbara with Sansum Clinic, Santa Barbara, California, United States

Central Coast Medical Oncology Corporation, Santa Maria, California, United States

Smilow Cancer Hospital at Yale-New Haven, New Haven, Connecticut, United States

Florida Cancer Specialists, Fort Myers, Florida, United States

Florida Cancer Specialists and Research Institute, Saint Petersburg, Florida, United States

H Lee Moffitt Cancer Center, Tampa, Florida, United States

Fort Wayne Oncology & Hematology, Fort Wayne, Indiana, United States

Cancer Center of Kansas, Wichita, Kansas, United States

Nebraska Methodist Hospital, Omaha, Nebraska, United States

Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, United States

Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, United States

Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

Monter Cancer Center, Lake Success, New York, United States

Thomas Jefferson University, Philadelphia, Pennsylvania, United States

UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, United States

Medical University of South Carolina, Charleston, South Carolina, United States

Sanford Research/USD, Sioux Falls, South Dakota, United States

Chattanooga Oncology Hematology Associates, Chattanooga, Tennessee, United States

Sarah Cannon Research Institute SCRI, Nashville, Tennessee, United States

Tennessee Oncology PLLC, Nashville, Tennessee, United States

Vanderbilt University Medical Center, Nashville, Tennessee, United States

Univ of Texas Health Science Center at San Antonio, San Antonio, Texas, United States

University of Utah School of Medicine, Salt Lake City, Utah, United States

University of Wisconsin-Madison Hospital and Health Clinic, Madison, Wisconsin, United States

Charité Campus Virchow-Klinikum, Berlin, , Germany

Hospital Universitari Vall d'Hebron, Barcelona, , Spain

Contact Details

Name: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Affiliation: Eli Lilly and Company

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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