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Spots Global Cancer Trial Database for A Study of CG-806 in Patients With Relapsed or Refractory CLL/SLL or Non-Hodgkin's Lymphomas

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Trial Identification

Brief Title: A Study of CG-806 in Patients With Relapsed or Refractory CLL/SLL or Non-Hodgkin's Lymphomas

Official Title: A Phase Ia/b Trial to Evaluate the Safety and Tolerability of CG-806 in Patients With CLL/SLL or Non-Hodgkin's Lymphomas

Study ID: NCT03893682

Interventions

CG-806

Study Description

Brief Summary: This study is being done to evaluate the safety, tolerability and effectiveness of Oral CG-806 for the treatment of patients with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), or Non-Hodgkin's Lymphomas who have failed or are intolerant to two or more lines of established therapy or for whom no other treatment options are available.

Detailed Description: This is a multicenter, open-label, Phase Ia/b dose escalation study of safety, pharmacodynamics, and pharmacokinetics of CG-806 in ascending cohorts (3+3 design) to determine the MTD or recommended dose in patients with relapsed or refractory CLL/SLL or Non-Hodgkin's Lymphoma patients. This is to be followed by a cohort expansion phase at the MTD or recommended oral dose.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of California Los Angeles, Los Angeles, California, United States

Pacific Cancer Care, Monterey, California, United States

Torrance Memorial Physician Network, Redondo Beach, California, United States

UCSD Moores Cancer Center, San Diego, California, United States

Sharp Clinical Oncology Research, San Diego, California, United States

Ridley-Tree Cancer Center, Santa Barbara, California, United States

St. Joseph Heritage Heathcare, Santa Rosa, California, United States

Rocky Mountain Cancer Centers, Aurora, Colorado, United States

Mayo Clinic Jacksonville, Jacksonville, Florida, United States

Orlando Health, Orlando, Florida, United States

Fort Wayne Medical Oncology and Hematology, Fort Wayne, Indiana, United States

University of Maryland, Greenebaum Comprehensive Cancer Center, Baltimore, Maryland, United States

The Center for Cancer and Blood Disorders a division of American Oncology Partners of Maryland, PA, Bethesda, Maryland, United States

UMass Memorial Medical Center, Worcester, Massachusetts, United States

University of Michigan, Ann Arbor, Michigan, United States

Mayo Clinic Rochester, Rochester, Minnesota, United States

SCL Health, St. Vincent Frontier Cancer Center, Billings, Montana, United States

Morristown Medical Center, Morristown, New Jersey, United States

Manhattan Hematology Oncology, New York, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Prisma Health - ITOR, Greenville, South Carolina, United States

Carolina Blood and Cancer Care Associates, Rock Hill, South Carolina, United States

Texas Oncology - Austin-Midtown, Austin, Texas, United States

Texas Oncology - Baylor Charles A. Sammons Cancer Center, Dallas, Texas, United States

Texas Oncology - Fort Worth Cancer Center, Fort Worth, Texas, United States

University of Texas, M.D. Anderson Cancer Center, Houston, Texas, United States

University of Texas Health Science Center at San Antonio, Mays Cancer Center, San Antonio, Texas, United States

Texas Oncology - Tyler, Tyler, Texas, United States

Virginia Oncology Associates, Norfolk, Virginia, United States

Northwest Cancer Specialists, P.C. - Compass Oncology, Vancouver, Washington, United States

Contact Details

Name: Rafael Bejar, MD, PhD

Affiliation: Aptose Biosciences Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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