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Helping You Prescribe Better

Genetic testing that accurately identifies genetic variants supported by drug labels and clinical guidelines to help physicians select the right therapy, at the right dose. 

Meet Dr. Dixon

Why PGx?

The trial-and-error method of selecting drug therapies

Failed Therapies
- 2 out of 3 patients fail the first medication prescribed

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Adverse Drug Reactions

- 4th leading cause of death in the U.S

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Costs to the Healthcare system

- $530B/yr attributed to non-optimized medication

Genetics are a significant driver in therapy response

Accounts for 20-95% of drug response variability
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PGx testing reduces ADRs by 52%

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Decreases the number of drugs and time to finding an efficacious treatment

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Design and
Performance

Comprehensive Test Panel

Test for 77 genetic variants in 21 of the most relevant pharmacogenetic genes

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Validated on platform optimized for PGx testing

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Reduce QNS with low DNA input

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CYP2D6 CNV and Hybrid Allele Detection

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Prevalence​

- 13% of the US population has a CYP2D6 CNV​

- Up to 45% of population has a non-functional hybrid allele

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PharmGx Assay Design

- Interrogates 7 regions across CYP2D6 and CYP2D7 pseudogene

  • Hybrid allele detection

  • High confidence CYP2D6 CNV detection

Result Interpretation

Clinical decision support for more than 100 medications

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Supported by drug labels and clinical guidelines

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Personalized results for every patient

Ease and Convenience

Simple process from ordering to reporting

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Fast TATs

Patient

Access

Notifications for out-of-pocket estimates > $200

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Low-cost cash pay and payment plans

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Financial assistance program

Physician Support

PharmD clinical support on demand

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Help interpret and advise on results

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Answer questions about PharmGx testing

For more details, contact us

Call 

949-418-8998 

Email 

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