1
Participants
Start Date
October 17, 2019
Primary Completion Date
July 22, 2020
Study Completion Date
July 29, 2020
Safety Laboratories
Complete blood cell count (CBC) w Differential, comprehensive metabolic panel (CMP), Prothrombin time/international normalized ratio (PT/INR) Activated Partial Thromboplastin Time (aPTT), Urinalysis
AE Assessment
Assessment of Adverse Events (AE)
Physical Exam
Physical Exam, Weight, Vital Signs, Eastern Cooperative Oncology Group (ECOG) Performance Status
Concomitant Medication Review
Prior and Concomitant Medication Review
Tumor Imaging
Tumor CT or MRI
nab-paclitaxel (Abraxane)/gemcitabine (Gemzar) Protocol Plus Disulfiram/Copper Gluconate
nab-paclitaxel (Abraxane)/gemcitabine (Gemzar) regimen Plus Disulfiram/Copper Gluconate dispensing
FOLFIRINOX regimen Plus Disulfiram/Copper Gluconate
FOLFIRINOX regimen Plus Disulfiram/Copper Gluconate dispensing
Single-agent gemcitabine (Gemzar) regimen Plus Disulfiram/Copper Gluconate
Single-agent gemcitabine (Gemzar) regimen Plus Disulfiram/Copper Gluconate dispensing
HonorHealth Research Institute, Scottsdale
Lead Sponsor
Collaborators (1)
Cantex Pharmaceuticals
INDUSTRY
HonorHealth Research Institute
OTHER