Trial Details 48 Total Sites

A Study Evaluating Targeted Therapies in Participants Who Have Advanced Solid Tumors With Genomic Alterations or Protein Expression Patterns Predictive of Response

This is a Phase II, multicenter, non-randomized, open-label, multi-arm study designed to evaluate the safety and efficacy of targeted therapies as single agents or in rational, specified combinations in participants with advanced unresectable or metastatic solid tumors determined to harbor specific biomarkers. Patients will be enrolled based on local testing performed at a Clinical Laboratory Improvement Amendments (CLIA)-certified or equivalently accredited diagnostic laboratory. The multi-arm structure of the MyTACTIC study allows patients with solid tumors to be treated with a drug or drug regimen tailored to their biomarker identified at screening.

New York City, New York
facility
Central Park Hematology and Oncology
1 facility
Recruiting
Los Angeles, California
facility
Los Angeles Hematology Oncology Medical Group
1 facility
Recruiting
San Jose, California
facility
Kaiser Permanente - San Jose Medical Center
1 facility
Recruiting
San Francisco, California
facility
Kaiser Permanente - San Francisco Medical Center
1 facility
Recruiting
Columbus, Ohio
facility
Mark H. Zangmeister Center
1 facility
Recruiting
Fort Worth, Texas
facility
The Center for Cancer and Blood Disorders - PPDS
1 facility
Recruiting
Detroit, Michigan
facility
Ascension St. John Hospital
1 facility
Recruiting
Memphis, Tennessee
facility
The West Clinic, PC dba West Cancer Center
1 facility
Recruiting
Portland, Oregon
facility
Kaiser Permanente Center For Health Research
1 facility
Recruiting
Baltimore, Maryland
facility
Saint Agnes Hospital - Baltimore - Hunt - PPDS
1 facility
Recruiting
Nashville, Tennessee
facility
Sarah Cannon Research Institute
1 facility
Recruiting
Sacramento, California
facility
Kaiser Permanente - Sacramento Medical Center and Medical Offices
1 facility
Recruiting