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Spots Global Cancer Trial Database for Rovalpituzumab Tesirine in Delta-Like Protein 3-Expressing Advanced Solid Tumors

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Trial Identification

Brief Title: Rovalpituzumab Tesirine in Delta-Like Protein 3-Expressing Advanced Solid Tumors

Official Title: An Open-Label Study of Rovalpituzumab Tesirine in Subjects With Delta-Like Protein 3-Expressing Advanced Solid Tumors

Study ID: NCT02709889

Study Description

Brief Summary: The primary objective of this study is to assess the safety and tolerability of rovalpituzumab tesirine in subjects with specific delta-like protein 3-expressing advanced solid tumors.

Detailed Description: This is a multicenter, open-label study involving multiple specific advanced solid tumor types, consisting of a dose escalation part A followed by an expansion part B. Cancer subtypes will be studied in separate disease-specific cohorts in both Parts. Eight separate cohorts will enroll malignant melanoma, medullary thyroid cancer (MTC), glioblastoma, large cell neuroendocrine carcinoma (LCNEC), neuroendocrine prostate cancer (NEPC), high-grade gastroenteropancreatic neuroendocrine carcinoma (GEP NEC), other NEC, and solid tumors other than the above.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Banner MD Anderson Cancer Ctr /ID# 155424, Gilbert, Arizona, United States

Mayo Clinic - Scottsdale /ID# 155419, Scottsdale, Arizona, United States

University of California, Los Angeles /ID# 155429, Los Angeles, California, United States

Univ California, San Francisco /ID# 155409, San Francisco, California, United States

Cedars-Sinai Medical Center - West Hollywood /ID# 155428, West Hollywood, California, United States

Univ of Colorado Cancer Center /ID# 155415, Aurora, Colorado, United States

Sarah Cannon Research Institute at HealthONE - Denver /ID# 155420, Denver, Colorado, United States

University of Florida - Archer /ID# 155414, Gainesville, Florida, United States

Moffitt Cancer Center /ID# 170220, Tampa, Florida, United States

Emory University Hospital /ID# 155417, Atlanta, Georgia, United States

University of Kentucky Chandler Medical Center /ID# 155423, Lexington, Kentucky, United States

Johns Hopkins University /ID# 155412, Baltimore, Maryland, United States

Massachusetts General Hospital /ID# 155411, Boston, Massachusetts, United States

Dana-Farber Cancer Institute /ID# 171044, Boston, Massachusetts, United States

Mayo Clinic - Rochester /ID# 155416, Rochester, Minnesota, United States

Washington University-School of Medicine /ID# 155425, Saint Louis, Missouri, United States

Rutgers Cancer Institute of NJ /ID# 162010, New Brunswick, New Jersey, United States

University of New Mexico /ID# 205054, Albuquerque, New Mexico, United States

Roswell Park Comprehensive Cancer Center /ID# 162015, Buffalo, New York, United States

Weill Cornell Medical College /ID# 155418, New York, New York, United States

Duke University Medical Center /ID# 155421, Durham, North Carolina, United States

Univ Hosp Cleveland /ID# 155410, Cleveland, Ohio, United States

Oregon Health and Science University /ID# 162011, Portland, Oregon, United States

Greenville Hospital System /ID# 155427, Greenville, South Carolina, United States

Mary Crowley Cancer Research /ID# 162014, Dallas, Texas, United States

Texas Oncology - Forth Worth /ID# 162045, Fort Worth, Texas, United States

University of Texas MD Anderson Cancer Center /ID# 155413, Houston, Texas, United States

University of Utah /ID# 155426, Salt Lake City, Utah, United States

Virginia Cancer Specialists /ID# 162006, Fairfax, Virginia, United States

Northwest Cancer Specialists, P.C. /ID# 155431, Vancouver, Washington, United States

Contact Details

Name: AbbVie Inc.

Affiliation: AbbVie

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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