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The purpose of this study is to enhance the understanding of the impact of genetic variants on individuals of Hispanic/Latino ancestry, especially as the variants pertain to the efficacy and safety of medications. The patient specimen is genotyped using a proprietary, carefully curated pharmacogenetic variant panel to determine the individual's phenotype. The Lighthouse report (PGx findings) are provided to the clinician, and a notification is generated when the patient has a genotype with a deleterious drug-metabolizing phenotype.
Principal Investigator | Herschl B. Silberman, MD |
Co-PI | Victoria Mancillas |
Sponsor | Cipherome |
Type of Trial | Interventional |