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Personalized Warfarin Dosing by Genomics and Computational Intelligence

Personalized Warfarin Dosing Using Genomics and Computational Intelligence

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00872079
Enrollment
175
Registered
2009-03-31
Start date
2008-09-30
Completion date
2011-09-30
Last updated
2014-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation, Myocardial Infarction, Venous Thrombosis

Keywords

warfarin, pharmacokinetics, pharmacodynamics

Brief summary

This study will create a computer program that can be used to help dose a drug called warfarin for the prevention of blood clotting. The study will collected specific information about those patients receiving this drug and use that information to create a computer program that will predict the effects of the drug. With this prediction program in place, the investigators can perform a series of what if I gave this amount of drug simulations to determine the best dose of drug for that patient. Once the computer programs are developed, the investigators will test the program in patients that actually need this drug. They will also include genetic information into the prediction since it has been shown that this information can affect how well the drug works. Patients will have this genetic information determined during this study.

Detailed description

The objective of this project is to develop new techniques to incorporate genomic data into pharmacodynamic models to improve the dosing of chronically administered drugs. Specifically, the investigators look to improve warfarin therapy by decreasing the variability in the effect of this drug using information about the subjects genotype and computational intelligence. The investigators propose to achieve our objectives using a prospective, randomized, controlled clinical trial of a computer program that they will develop from both historical and prospective data. This computer program will be tested against a control group using standard warfarin dosing, and a group using standard dosing plus subject genotype. Warfarin dose and response data will be obtained from patients seen in the Louisville VA anticoagulation clinic. Following informed consent, subject genotype for cytochrome P450 allele 2C9 (2C9) and vitamin K epoxide reductase complex subunit 1 (VKORC1) will be determined. Other data routinely obtained to aid in warfarin dosing will also be recorded. Using this information, the investigators will develop many different models for warfarin dosing using incrementally more information. Each of these models will be tested using computer simulation until they have obtained the best model. This model will be used in a pilot study to test performance in real time. The results of the pilot study will then be used to power a final clinical trial of standard dosing, standard dosing and genetic information, computer dosing, and computer dosing plus genetic information. The specific aims of this research are: 1. Determine the structure and the type of neural network model for predictions from historically obtained data. (Computer Model) 2. Prospectively develop an individualized neural network and nonlinear mixed effect modelling (NONMEM) model capable of predicting erythropoietin dosing for chronic in-center hemodialysis patients using adaptive techniques. 3. Develop computer programs based on neural computing that can be used in a clinical setting. (Computer Model) 4. Determine the utility of the computer programs prospectively in the clinical setting.

Interventions

DEVICEGenomics

Model predictive control is a computer based algorithm that can be applied to drug dosing. This computer tool uses a model of how a patient will respond to a drug dose based on demographic and historical dosing information to predict a new drug response. A drug dose controller applies all possible doses to the response model and selects the one dose that best meets the stated goals of the drug therapy. In the case of warfarin, we will calculate an international normalized ratio (INR) value within a specific target range.

Sponsors

US Department of Veterans Affairs
Lead SponsorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Warfarin therapy * Attend anticoagulation clinic * Warfarin therapy for 6 months

Exclusion criteria

* History of non-compliance

Design outcomes

Primary

MeasureTime frameDescription
Patient GenomicsBaselineDuring Aim 2, Determined Patient Genotypes: CYP2C9 and VKORC1.

Countries

United States

Participant flow

Pre-assignment details

Participants were not enrolled into the randomized clinical trial for Aim 4 due to lack of funding.

Participants by arm

ArmCount
Genomics
The specific aims of this research are: 1. Determine the structure and the type of neural network model for predictions from historically obtained data. (Computer Model) 2. Prospectively develop an individualized neural network and NONMEM model capable of predicting erythropoietin dosing for chronic in-center hemodialysis patients using adaptive techniques. 3. Develop computer programs based on neural computing that can be used in a clinical setting. (Computer Model) 4. Determine the utility of the computer programs prospectively in the clinical setting.
175
Total175

Baseline characteristics

CharacteristicGenomics
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
125 Participants
Age, Categorical
Between 18 and 65 years
50 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
17 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
1 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
157 Participants
Sex: Female, Male
Female
10 Participants
Sex: Female, Male
Male
165 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 0
serious
Total, serious adverse events
0 / 0

Outcome results

Primary

Patient Genomics

During Aim 2, Determined Patient Genotypes: CYP2C9 and VKORC1.

Time frame: Baseline

ArmMeasureGroupValue (NUMBER)
GenomicsPatient GenomicsCYP2C9: *1/*1112 participants
GenomicsPatient GenomicsCYP2C9: *1/*223 participants
GenomicsPatient GenomicsCYP2C9: *1/*319 participants
GenomicsPatient GenomicsCYP2C9: *2/*23 participants
GenomicsPatient GenomicsCYP2C9: *2/*33 participants
GenomicsPatient GenomicsCYP2C9: *3/*32 participants
GenomicsPatient GenomicsCYP2C9: Not Determined13 participants
GenomicsPatient GenomicsVKORC1: AA23 participants
GenomicsPatient GenomicsVKORCI:GA72 participants
GenomicsPatient GenomicsVKORCI:GG67 participants
GenomicsPatient GenomicsVKORCI: Not Determined13 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026