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Spots Global Cancer Trial Database for A Study of Prexasertib (LY2606368) in Platinum-Resistant or Refractory Recurrent Ovarian Cancer

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Trial Identification

Brief Title: A Study of Prexasertib (LY2606368) in Platinum-Resistant or Refractory Recurrent Ovarian Cancer

Official Title: A Phase 2 Study of Prexasertib in Platinum-Resistant or Refractory Recurrent Ovarian Cancer

Study ID: NCT03414047

Conditions

Ovarian Cancer

Interventions

Prexasertib

Study Description

Brief Summary: The purpose of this study is to evaluate the efficacy and safety of prexasertib in women with platinum-resistant or refractory recurrent ovarian cancer.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Arizona Oncology Associates, P.C., Tucson, Arizona, United States

Kaiser Permanente Medical Center, Vallejo, California, United States

University of Southern Florida School of Medicine, Gainesville, Florida, United States

Dana Farber Cancer Institute, Boston, Massachusetts, United States

Research Medical Center, Kansas City, Missouri, United States

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

Cancer Care Associates, Tulsa, Oklahoma, United States

Thomas Jefferson University, Philadelphia, Pennsylvania, United States

Rhode Island Hospital, Providence, Rhode Island, United States

Sioux Valley Clinic, Sioux Falls, South Dakota, United States

University of Tennessee Medical Center, Knoxville, Tennessee, United States

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

Tennessee Oncology PLLC, Nashville, Tennessee, United States

Seattle Cancer Care Alliance, Seattle, Washington, United States

Concord Repatriation General Hospital, Concord, New South Wales, Australia

Prince of Wales Hospital, Randwick, New South Wales, Australia

Westmead Hospital, Wentworthville, New South Wales, Australia

Royal Brisbane and Womens Hospital, Herston, Queensland, Australia

Mater Adult Hospital Brisbane, South Brisbane, Queensland, Australia

Flinders Medical Centre, Bedford Park, South Australia, Australia

Burnside War Memorial Hospital, Toorak Gardens, South Australia, Australia

Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

Institut Jules Bordet, Brussel, , Belgium

Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg, Leuven, , Belgium

GZA St Augustinus, Wilrijk, , Belgium

Rambam Medical Center, Haifa, , Israel

Shaare Zedek Medical Center, Jerusalem, , Israel

Sheba Medical Center, Ramat Gan, , Israel

Policlinico Univ. Agostino Gemelli, Roma, Lazio, Italy

Istituto Europeo di Oncologia, Milano, Milan, Italy

Istituto Tumori Fondazione G. Pascale IRCCS, Napoli, Naples, Italy

Samsung Medical Center, Seoul, Korea, Korea, Republic of

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

Asan Medical Center, Seoul, , Korea, Republic of

Severance Hospital Yonsei University Health System, Seoul, , Korea, Republic of

Hospital Universitari Vall d'Hebron, Barcelona, , Spain

Hospital Reina Sofia, Cordoba, , Spain

Hospital Universitario Ramon y Cajal, Madrid, , Spain

Hospital Universitario 12 de Octubre, Madrid, , Spain

Hospital Universitario La Paz, Madrid, , Spain

University College Hospital - London, London, Greater London, United Kingdom

Christie NHS Foundation Trust, Manchester, Greater Manchester, United Kingdom

Mount Vernon Hospital, Northwood, Middlesex, United Kingdom

Royal Surrey County Hospital, Guildford, Surrey, United Kingdom

Royal Marsden Hospital, Sutton, Surrey, United Kingdom

Northampton General Hospital, Northampton, , United Kingdom

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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