Systems and methods for personalized de-risking based on patient genome data
First Claim
1. A method for personalized de-risking of medications based on multi-variate analysis of genomic information of a patient and adverse event data of combination therapies, comprising:
- receiving, by a multi-variate analyzer executed by a processor of a computing device from a user, an identification of a genomic variant of a patient altering activity of a first protein and an identification of a second medication targeting a second protein to be prescribed to the patient;
identifying, by the multi-variate analyzer by querying a medication information database, responsive to receiving the identification of the genomic variant, a first medication targeting the first protein;
retrieving, by the multi-variate analyzer by querying an adverse event database, a number of adverse event records each comprising an identification of co-medication of the first medication and the second medication, and an identification of an adverse event, wherein the first medication targets said first protein whose activity is altered by said genomic variant;
performing, by the multi-variate analyzer, a multi-variate analysis comprising;
determining, by the multi-variate analyzer based on the retrieved number of adverse event records, a likelihood of an adverse event occurring through co-medication of the first medication and the second medication, anddetermining, by the multi-variate analyzer, that an adverse event corresponding to co-medication of the first medication and the second medication is likely to occur if the patient is prescribed the second medication and is not prescribed the first medication, responsive to the identified likelihood of an adverse event occurring through co-medication of the first medication and the second medication and the identification of the genomic variant of the patient; and
displaying, by a display module executed by computing device, the second medication as contraindicated responsive to the determination.
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Accused Products
Abstract
The present disclosure describes systems and methods for using patient-specific genomic information to optimize or de-risk therapy for the patient. A user may identify a medication for consideration for prescription to a patient, and a genetic variant of the patient affecting a first protein. An analyzer may identify a second medication targeting the first protein, and may retrieve adverse event data from an adverse event database for patients co-medicated with both the first medication and second medication. The analyzer may determine, based on rates of adverse events, the likelihood of an adverse event occurring through co-medication of the first medication and second medication. Based on the likelihood, and based on a correspondence or non-correspondence between a protein activation characteristic of the first medication and the effect of the genetic variant of the patient, the analyzer may indicate or contra-indicate the first medication for the patient.
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Citations
23 Claims
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1. A method for personalized de-risking of medications based on multi-variate analysis of genomic information of a patient and adverse event data of combination therapies, comprising:
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receiving, by a multi-variate analyzer executed by a processor of a computing device from a user, an identification of a genomic variant of a patient altering activity of a first protein and an identification of a second medication targeting a second protein to be prescribed to the patient; identifying, by the multi-variate analyzer by querying a medication information database, responsive to receiving the identification of the genomic variant, a first medication targeting the first protein; retrieving, by the multi-variate analyzer by querying an adverse event database, a number of adverse event records each comprising an identification of co-medication of the first medication and the second medication, and an identification of an adverse event, wherein the first medication targets said first protein whose activity is altered by said genomic variant; performing, by the multi-variate analyzer, a multi-variate analysis comprising; determining, by the multi-variate analyzer based on the retrieved number of adverse event records, a likelihood of an adverse event occurring through co-medication of the first medication and the second medication, and determining, by the multi-variate analyzer, that an adverse event corresponding to co-medication of the first medication and the second medication is likely to occur if the patient is prescribed the second medication and is not prescribed the first medication, responsive to the identified likelihood of an adverse event occurring through co-medication of the first medication and the second medication and the identification of the genomic variant of the patient; and displaying, by a display module executed by computing device, the second medication as contraindicated responsive to the determination. - View Dependent Claims (2, 3, 4, 5, 21, 22, 23)
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6. A method for personalized de-risking of medications based on genomic information of a patient and adverse event data of combination therapies, comprising:
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receiving, by an analyzer executed by a processor of a computing device from a user, an identification of a genomic variant of a patient altering activity of a first protein and an identification of a second medication targeting a second protein to be prescribed to the patient; identifying, by the analyzer by querying a medication information database, responsive to receiving the identification of the genomic variant, a first medication targeting the first protein; retrieving, by the analyzer by querying an adverse event database, a number of adverse event records each comprising an identification of co-medication of the first medication and the second medication, and an identification of an adverse event, wherein the first medication targets said first protein whose activity is altered by said genomic variant; determining, by the analyzer based on the retrieved number of adverse event records, a likelihood of an adverse event occurring through co-medication of the first medication and the second medication; determining, by the analyzer responsive to the identified likelihood of an adverse event occurring through co-medication of the first medication and the second medication and the identification of the genomic variant of the patient, that an adverse event corresponding to co-medication of the first medication and the second medication is not likely to occur if the patient is prescribed the second medication and is not prescribed the first medication; and displaying, by a display module executed by the computing device, the second medication as indicated, responsive to the determination. - View Dependent Claims (7, 8, 9, 10)
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11. A system for personalized de-risking of medications based on genomic information of a patient and adverse event data of combination therapies, comprising:
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a computing device comprising a processor executing an analyzer, configured for receiving, from a user, an identification of a genomic variant of a patient altering activity of a first protein and an identification of a second medication targeting a second protein to be prescribed to the patient, identifying, by querying a medication information database, responsive to receiving the identification of the genomic variant, a first medication targeting the first protein, retrieving, by querying an adverse event database, a number of adverse event records each comprising an identification of co-medication of the first medication and the second medication, and an identification of an adverse event, wherein the first medication targets said first protein whose activity is altered by said genomic variant, determining, based on the retrieved number of adverse event records, a likelihood of an adverse event occurring through co-medication of the first medication and the second medication, and determining that an adverse event corresponding to co-medication of the first medication and the second medication is likely to occur if the patient is prescribed the second medication and is not prescribed the first medication, responsive to the identified likelihood of an adverse event occurring through co-medication of the first medication and the second medication and the identification of the genomic variant of the patient; and a display module, configured for displaying to the user the second medication as contraindicated responsive to the determination. - View Dependent Claims (12, 13, 14, 15)
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16. A system for personalized de-risking of medications based on genomic information of a patient and adverse event data of combination therapies, comprising:
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a computing device comprising a processor executing an analyzer, configured for receiving from a user, an identification of a genomic variant of a patient altering activity of a first protein and an identification of a second medication targeting a second protein to be prescribed to the patient, identifying, by querying a medication information database, responsive to receiving the identification of the genomic variant, a first medication targeting the first protein, retrieving, by querying an adverse event database, a number of adverse event records each comprising an identification of co-medication of the first medication and the second medication, and an identification of an adverse event, wherein the first medication targets said first protein whose activity is altered by said genomic variant, determining, based on the retrieved number of adverse event records, a likelihood of an adverse event occurring through co-medication of the first medication and the second medication, and determining, responsive to the identified likelihood of an adverse event corresponding to co-medication of the first medication and the second medication occurring through co-medication of the first medication and the second medication and the identification of the genomic variant of the patient, that an adverse event is not likely to occur if the patient is prescribed the second medication and is not prescribed the first medication; and a display module configured for displaying, to the user, the second medication as indicated, responsive to the determination. - View Dependent Claims (17, 18, 19, 20)
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Specification