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Spots Global Cancer Trial Database for A Dose Escalation and Cohort Expansion Study of KB-0742 in Participants With Relapsed or Refractory Solid Tumors or Non-Hodgkin Lymphoma

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Trial Identification

Brief Title: A Dose Escalation and Cohort Expansion Study of KB-0742 in Participants With Relapsed or Refractory Solid Tumors or Non-Hodgkin Lymphoma

Official Title: Phase 1, First-in-human, Open-label Dose Escalation and Cohort Expansion Study of KB-0742 in Patients With Relapsed or Refractory Solid Tumors or Non-Hodgkin Lymphoma

Study ID: NCT04718675

Interventions

KB-0742

Study Description

Brief Summary: Part 1: Dose Escalation. The primary objective of Part 1 of this study is to evaluate the safety and tolerability of KB-0742 in participants with relapsed or refractory (R/R) solid tumors or non-Hodgkin lymphoma (NHL). Part 2: Cohort Expansion. The primary objective of Part 2 of this study is to further evaluate the safety and tolerability of KB-0742 in defined participant cohorts.

Detailed Description:

Eligibility

Minimum Age: 12 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

City of Hope, Duarte, California, United States

MemorialCare - Orange Coast Medical Center, Fountain Valley, California, United States

City of Hope - Orange County Lennar Foundation Cancer Center, Irvine, California, United States

Precision NextGen Oncology, Los Angeles, California, United States

Norris Comprehensive Cancer Center, Los Angeles, California, United States

Cedars Sinai, Los Angeles, California, United States

University of California, Los Angeles (UCLA), Los Angeles, California, United States

Community Health Network Community Cancer Center South, Indianapolis, Indiana, United States

Community Health Network Community Cancer Center North, Indianapolis, Indiana, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Dana Farber Cancer Institute, Boston, Massachusetts, United States

University of Michigan Rogel Cancer Center, Ann Arbor, Michigan, United States

Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, United States

Washington University, Saint Louis, Missouri, United States

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

Pennsylvania Cancer Specialists Research Institute - Gettysburg Cancer Center, Gettysburg, Pennsylvania, United States

Thomas Jefferson University, Philadelphia, Pennsylvania, United States

SCRI Tennessee Oncology, Nashville, Tennessee, United States

Oncology Consultants Texas Medical Center, Houston, Texas, United States

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

South Texas Accelerated Research Therapeutics, San Antonio, Texas, United States

Virginia Cancer Specialists, Fairfax, Virginia, United States

Hospital Clinic de Barcelona, Barcelona, , Spain

Hospital Clínico San Carlos, Madrid, , Spain

Hospital Universitario Quirónsalud Madrid, Madrid, , Spain

Sarah Cannon Research Institute London, London, , United Kingdom

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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