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Spots Global Cancer Trial Database for A Placebo-Controlled Study of Saracatinib (AZD0530) in Patients With Recurrent Osteosarcoma Localized to the Lung

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Trial Identification

Brief Title: A Placebo-Controlled Study of Saracatinib (AZD0530) in Patients With Recurrent Osteosarcoma Localized to the Lung

Official Title: A Randomized, Double-Blinded, Placebo-Controlled, Multi-Institutional, Cross-over, Phase II.5 Study of Saracatinib (AZD0530), a Selective Src Kinase Inhibitor, In Patients With Recurrent Osteosarcoma Localized to the Lung

Study ID: NCT00752206

Conditions

Osteosarcoma

Interventions

Saracatinib
Placebo

Study Description

Brief Summary: The purpose of this study is to determine how long patients who undergo complete surgical removal of recurrent osteosarcoma in the lung will remain free of cancer after taking Saracatinib compared to patients taking placebo (a sugar pill).

Detailed Description: Further details provided by SARC (Sarcoma Alliance for Research through Collaboration): After complete surgical removal of their cancer, patients will be randomly assigned to receive either Saracatinib or placebo (a sugar pill) throughout the study. Patients will take Saracatinib (or placebo) once daily by mouth for a total of 364 days. The duration of treatment is divided into 13 cycles, 28 days each cycle with no breaks in between. Patients will be seen for interim medical history, physical exam and laboratory studies prior to each cycle. To monitor for recurrence of tumor, patients will undergo thoracic CT scans at 3-4 weeks, 6-8 weeks, at 3 months, at 6 months, at 9 months, at 12 months, then every 6 months up to 2 years, and then every year up to 5 years after starting treatment. An electrocardiogram (ECG) will be taken at 3 months, and a bone scan will be performed at 12 months. Patients who recur in the lung while on-study and who are thought to be amenable to complete surgical resection will be able to find out if they were receiving placebo or saracatinib. Those patients who were receiving placebo may then have the option of undergoing surgical resection. If fully resected of all recurrent disease,they will be given the option of receiving oral therapy with saracatinib. Saracatinib will be administered as a once daily, oral dose of 175 mg, for a 28-day cycle, with no breaks between cycles. The duration of treatment with saracatinib will be thirteen 28-day cycles (364 days total). If complete resection of all lung nodules is not achieved, the patient will be removed from the study. Patients who recur in locations other than the lung while on-study will be taken off study at that time. Blood and tumor samples for research purposes will be collected at the time the tumor is removed. After completing all 13 cycles, patients will be followed for approximately every 3 months until 2 years from starting treatment, then approximately every 6 months until 4 years from starting treatment, and once at year 5.

Eligibility

Minimum Age: 15 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama, Birmingham, Alabama, United States

Children's Hospital Los Angeles, Los Angeles, California, United States

USC/Norris Comprehensive Cancer Center and Hospital, Los Angeles, California, United States

UCLA/Mattel's Children's Hospital, Los Angeles, California, United States

Stanford University, Palo Alto, California, United States

UCSF, San Francisco, California, United States

Sarcoma Oncology Center, Santa Monica, California, United States

University of Florida, Gainesville, Florida, United States

University of Miami, Miami, Florida, United States

Indiana University, Indianapolis, Indiana, United States

University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States

National Cancer Institute, Bethesda, Maryland, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

University of Michigan, Ann Arbor, Michigan, United States

Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States

St. Jude Children's Research Hospital, Memphis, Tennessee, United States

Seattle Cancer Care Alliance/University of Washington Medical Center, Seattle, Washington, United States

Contact Details

Name: Kristin Baird, MD

Affiliation: National Cancer Institute - Pediatric Oncology Branch

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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