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Spots Global Cancer Trial Database for A Study of DSP-7888 Dosing Emulsion in Combination With Bevacizumab in Patients With Recurrent or Progressive Glioblastoma Following Initial Therapy

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Trial Identification

Brief Title: A Study of DSP-7888 Dosing Emulsion in Combination With Bevacizumab in Patients With Recurrent or Progressive Glioblastoma Following Initial Therapy

Official Title: A Randomized, Multicenter, Adaptive Phase 3 Study of DSP-7888 Dosing Emulsion in Combination With Bevacizumab Versus Bevacizumab Alone in Patients With Recurrent or Progressive Glioblastoma Following Initial Therapy (WIZARD 201G)

Study ID: NCT03149003

Conditions

Glioblastoma

Study Description

Brief Summary: This is an event driven, adaptive design, a randomized, active-controlled, multicenter, open-label, parallel groups, Phase 3 study of DSP-7888 Dosing Emulsion plus Bevacizumab versus Bevacizumab alone in patients with recurrent or progressive glioblastoma multiforme (GBM) following treatment with first line therapy consisting of surgery and radiation with or without chemotherapy.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

Center for Neurosciences, Tucson, Arizona, United States

Highlands Oncology Group, Fayetteville, Arkansas, United States

UCSD- Moores Cancer Center, La Jolla, California, United States

Kaiser Permanente Los Angeles Medical Center, Los Angeles, California, United States

Cedars Sinai Medical Center, Los Angeles, California, United States

Neuro-Oncology/ US Irvine Medical Center, Orange, California, United States

Sansum Clinic, Santa Barbara, California, United States

John Wayne Cancer Institute, Santa Monica, California, United States

Rocky Mountain Cancer Center, Denver, Colorado, United States

Piedmont brain tumor center, Atlanta, Georgia, United States

Rush University Medical Center, Chicago, Illinois, United States

University of Kentucky / Department of Internal Medicine / Markey Cancer Center, Lexington, Kentucky, United States

Norton Cancer Institute, Louisville, Kentucky, United States

Tufts Medical Center, Boston, Massachusetts, United States

Henry Ford Health System, Detroit, Michigan, United States

Abbott Northwestern Hospital, Minneapolis, Minnesota, United States

Hackensack University Medical Center, Hackensack, New Jersey, United States

Dent Neurosciences Research Center, Amherst, New York, United States

Weill Cornell Medicine, New York, New York, United States

Columbia University Medical Center/ Neurological Institute of NY, New York, New York, United States

University of Rochester Medical Center, Rochester, New York, United States

University Hospitals of Cleveland, Cleveland, Ohio, United States

Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, United States

University of Toledo, Toledo, Ohio, United States

Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center (UPMC), Pittsburgh, Pennsylvania, United States

Rhode Island Hospital, Providence, Rhode Island, United States

University of Tennessee Academic Medical Center Cancer Institute, Knoxville, Tennessee, United States

Texas Oncology Austin Midtown, Austin, Texas, United States

Baylor Scott and White, Dallas, Texas, United States

Houston Methodist, Houston, Texas, United States

Mischer Neuroscience Associates/Memorial Hermann Hospital, Houston, Texas, United States

Renovatio Clinical, The Woodlands, Texas, United States

Virginia Cancer Specialists, PC, Fairfax, Virginia, United States

Swedish Medical Center, Seattle, Washington, United States

University of Wisconsin Hospital, Madison, Wisconsin, United States

CancerCare Manitoba, Winnipeg, Manitoba, Canada

Montreal Neurological Institute and Hospital, Montreal, Quebec, Canada

University of Sherbrooke, Sherbrooke, Quebec, Canada

Hokkaido University Hospital, Sapporo, Hokkaido, Japan

Kagoshima University Hospital, Kagoshima-shi, Kagoshima, Japan

Niigata University Medical and Dental Hospital, Chuo Ku, Niigata, Japan

Osaka International Cancer Institute, Chuo Ku, Osaka, Japan

The University of Tokyo Hospital, Bunkyo-ku, Tokyo, Japan

National Cancer Center Hospital, Chuo-ku, Tokyo, Japan

Hiroshima University Hospital, Hiroshima, , Japan

Kumamoto University Hospital, Kumamoto, , Japan

University Hospital, Kyoto Prefectural University of Medicine, Kyoto, , Japan

National Hospital Organization Kyoto Medical Center, Kyoto, , Japan

Tokyo Women's Medical University Hospital, Shinjuku-Ku, , Japan

Yamagata University Hospital, Yamagata, , Japan

Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, Korea, Republic of

Seoul National University Hospital, Seoul, , Korea, Republic of

Severance Hospital, Seoul, , Korea, Republic of

Gangnam Severance Hospital, Seoul, , Korea, Republic of

Samsung Medical Center, Seoul, , Korea, Republic of

The Catholic University of Korea, Seoul St. Mary's Hospital, Seoul, , Korea, Republic of

China Medical University Hospital, Taichung, , Taiwan

National Taiwan University Hospital, Taipei, , Taiwan

Chang Gung Memorial Hospital, Taoyuan City, , Taiwan

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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