53
Participants
Start Date
January 1, 2018
Primary Completion Date
April 1, 2019
Study Completion Date
April 17, 2024
Genecept Assay and G-DIG decision tool
Participating providers will review results of the Genecept Assay using a secure web-based program and will utilize the G-DIG tool in order to determine the optimal medication regime for the patient, based on their individual genetic profile. Genomind will provide training to all investigators prior to the study start regarding the interpretation of the pharmacological assay and the use of the G-DIG tool. Genomind representatives will be available throughout the duration of the study for consultation regarding the interpretation and implementation of the testing results. All final decisions about changing dosage, adding medications, or removing medications will be determined by the provider.
VA Puget Sound Health Care System, Tacoma
Collaborators (1)
Genomind, LLC
INDUSTRY
Seattle Institute for Biomedical and Clinical Research
OTHER