Ex Vivo Drug Sensitivity Testing and Multi-Omics Profiling

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age1-21
SponsorFlorida International University

About this trial

Functional precision medicine (FPM) is a relatively new approach to cancer therapy based on direct exposure of patient- isolated tumor cells to clinically approved drugs and integrates ex vivo drug sensitivity testing (DST) and genomic profiling to determine the optimal individualized therapy for cancer patients. In this study, we will enroll relapsed or refractory pediatric cancer patients with tissue available for DST and genomic profiling from the South Florida area, which is 69% Hispanic and 18% Black. Tumor cells collected from tissue taken during routine biopsy or surgery will be tested.

Eligibility criteria

Qualifiers

Patients aged 21 years or younger at the time of enrollment on this study of any gender, race or ethnicity.

Disqualifiers

Subjects who do not have malignant tissue available and accessible The amount of excised malignant tissue is not sufficient for the ex vivo drug testing and/or genetic profiling.

Trial design

Treatments tested in this trial

  • Functional Precision Medicine

Treatment groups

65 Participants
are divided into 1 treatment group

Sponsors and collaborators

Florida International University

Lead sponsor

Nicklaus Children's Hospital f/k/a Miami Children's Hospital

Collaborator

First Ascent Biomedical Inc.

Collaborator

National Institute on Minority Health and Health Disparities (NIMHD)

Collaborator