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

Outcome

Outcome not reported

Stopped (Business): “funding - sponsor filing Chapter 11 bankruptcy”

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