drugset / Trial / NCT03432741

Direct Tumor Microinjection and FDG-PET in Testing Drug Sensitivity in Patients With Relapsed or Refractory Non-Hodgkin Lymphoma, Hodgkin Lymphoma, or Stage IV Breast Cancer

NCT03432741

Phase 1 Terminated 17 enrolled Mayo Clinic
NaSingle-groupOpen-labelTreatment

Summary

This pilot phase I trial studies the side effects of direct tumor microinjection and fludeoxyglucose F-18 positron emission tomography (FDG-PET) in testing drug sensitivity in patients with non-Hodgkin lymphoma, Hodgkin lymphoma, or stage IV breast cancer that has returned after a period of improvement or does not respond to treatment. Injecting tiny amounts of anti-cancer drugs directly into tumors on the skin or in lymph nodes and diagnostic procedures, such as FDG-PET, may help to show which drugs work better in treating patients with non-Hodgkin lymphoma, Hodgkin lymphoma, or breast cancer.

Timeline

Start
2018-03-27
Primary completion
2022-08-26
Completion
2022-10-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Belinostat Small molecule Other
Subject Carfilzomib Other / unclassified Other
Subject Copanlisib Small molecule Other
Subject Daratumumab Monoclonal antibody Other
Subject Gemcitabine Small molecule Other
Subject Nivolumab Monoclonal antibody Other
Subject Obinutuzumab Monoclonal antibody Other
Subject Pembrolizumab Monoclonal antibody Other
Subject Rituximab Monoclonal antibody Other
Subject Romidepsin Peptide Other
Subject Trastuzumab Monoclonal antibody Other