IP Library › Granted Patent US 10,570,452
Granted Patent B2
US 10,570,452 · App. 15/705,071 · Granted Feb 25, 2020

Method of predicting a predisposition to QT prolongation

Inventors: Christian Lavedan (Potomac, MD); Simona Volpi (Derwood, MD); Louis Licamele (Potomac, MD)
Assignee: VANDA PHARMACEUTICALS, INC.
C12Q1/6883C12Q2600/106C12Q2600/136C12Q2600/156
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Quick Facts
Patent No.
US 10,570,452
App. No.
15/705,071
Granted
Feb 25, 2020
Kind
B2
Abstract

The present invention describes an association between genetic polymorphisms in the BAI3 gene and a predisposition to prolongation of the QT interval, and provides related methods for the prediction of such a predisposition, the administration of QT interval-prolonging compounds to individuals having such a predisposition, and determining whether a compound is capable of inducing QT prolongation.

Claims (16)

1. A method of administering a compound to a human individual, wherein the compound is iloperidone, a metabolite of iloperidone, or a pharmaceutically acceptable salt of iloperidone or metabolite thereof, the method comprising:

determining the individual's BAI3 genotype at a single nucleotide polymorphism (SNP) locus selected from the group consisting of rs7776307, rs10944944, rs9294774, rs9360320, and rs10485427; and

administering a first quantity of the compound if the individual's BAI3 genotype is associated with increased risk of QT prolongation and is CT at rs7776307, AA at rs10944944, non-TT at rs9294774, non-AC at rs9360320, or AG at rs10485427, or

administering a second quantity of the compound if the individual's BAI3 genotype is non-CT at rs7776307, non-AA at rs10944944, TT at rs9294774, AC at rs9360320, or non-AG at rs10485427; wherein the first quantity of the compound is less than the second quantity of the compound.

2. The method of claim 1 , further comprising determining the individual's CYP2D6 genotype.

3. The method of claim 1 , wherein the compound is iloperidone or a pharmaceutically acceptable salt thereof.

4. A method of administering a compound to a human individual suffering from long QT syndrome (LQTS), wherein the compound is iloperidone, a metabolite of iloperidone, or a pharmaceutically acceptable salt of iloperidone or metabolite thereof, the method comprising:

determining the individual's BAI3 genotype at a single nucleotide polymorphism (SNP) locus selected from the group consisting of rs7776307, rs10944944, rs9294774, rs9360320, and rs10485427; and

administering a first quantity of the compound if the individual's BAI3 genotype is associated with increased risk of QT prolongation and is CT at rs7776307, AA at rs10944944, non-TT at rs9294774, non-AC at rs9360320, or AG at rs10485427, or

administering a second quantity of the compound if the individual's BAI3 genotype is non-CT at rs7776307, non-AA at rs10944944, TT at rs9294774, AC at rs9360320, or non-AG at rs10485427; wherein the first quantity of the compound is less than the second quantity of the compound.

5. The method of claim 4 , further comprising determining the individual's CYP2D6 genotype.

6. The method of claim 4 , wherein the compound is iloperidone or a pharmaceutically acceptable salt thereof.

7. The method of claim 1 , wherein the compound is a metabolite of iloperidone or a pharmaceutically acceptable salt thereof, wherein the metabolite is 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanol.

8. The method of claim 4 , wherein the compound is a metabolite of iloperidone or a pharmaceutically acceptable salt thereof, wherein the metabolite is 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanol.

9. The method of claim 1 , wherein the second quantity of the compound is 24 mg/day.

10. The method of claim 4 , wherein the second quantity of the compound is 24 mg/day.

Continuity (4)
Continuation 14694142 · Apr 23, 2015
Continuation 13263077
Provisional Application 61167140 · Apr 6, 2009
Related Publication 20180002758A1 · Jan 4, 2018
Cited By (1)
US 12,606,869