1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

26
Mechanism of Action Mechanism of Action Greg Beatch, Ph.D. Greg Beatch, Ph.D. Vice President, Scientific Affairs Vice President, Scientific Affairs Cardiome Pharma Corp. Cardiome Pharma Corp.

Transcript of 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

Page 1: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Mechanism of ActionMechanism of Action

Greg Beatch, Ph.D.Greg Beatch, Ph.D.Vice President, Scientific AffairsVice President, Scientific Affairs

Cardiome Pharma Corp.Cardiome Pharma Corp.

Page 2: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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VernakalantVernakalantMechanism of ActionMechanism of Action

• Multiple ion channel blockerMultiple ion channel blocker– Targeted to AFTargeted to AF

• Relatively atrial selectiveRelatively atrial selective

• Rapid conversion of atrial fibrillationRapid conversion of atrial fibrillation

• Pharmacologic effects consistent with Pharmacologic effects consistent with ion channel blocking profileion channel blocking profile

Page 3: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Blocks K+ Channels Vernakalant Blocks K+ Channels Important in Atrial RepolarizationImportant in Atrial Repolarization

Current IC50 (µM)

Ito 5-30

IKur 3-13

IKACh 10

IKr 7-21

IKs > 100

IK1 > 1000 100 200 300 400 ms

IKur

IKr

Ito

IKACh

0 mV

Fedida et al. J Cardiovasc Electrophysiol 2005Fedida et al. J Cardiovasc Electrophysiol 2005

Page 4: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Effects of Vernakalant on Effects of Vernakalant on Atrial Tissue from Humans with Atrial Tissue from Humans with

Atrial FibrillationAtrial Fibrillation

Control(n=7)

10 µM(n=7)

APD20 (ms) 25 ± 4 34 ± 6**

APD90 (ms) 229 ± 13 243 ± 16**

ERP (ms) 239 ± 11 259 ± 11**

Resting potential (mV) -76 ± 1 -74 ± 1

dV/dtmax (V/s) 244 ± 38 219 ± 32

Ravens et al. European Society of Cardiology 2007Ravens et al. European Society of Cardiology 2007

Data collected at 60 bpm; ** P<0.01Data collected at 60 bpm; ** P<0.01

Page 5: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Prolongs Atrial Vernakalant Prolongs Atrial Refractory Period: Human EP StudyRefractory Period: Human EP Study

* P<0.05 vs. baseline* P<0.05 vs. baseline

Dorian et al. J Cardiovasc Pharmacol 2007Dorian et al. J Cardiovasc Pharmacol 20074 mg/kg4 mg/kg

100 bpm pacing100 bpm pacing

**

0

10

20

30

40

AERP VERP

Ch

ang

e fr

om

Bas

elin

e (m

sec)

Page 6: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Data collected at 60 bpm; ** P<0.01Data collected at 60 bpm; ** P<0.01

Ravens et al. European Society of Cardiology 2007Ravens et al. European Society of Cardiology 2007

Effects of Vernakalant on Effects of Vernakalant on Atrial Tissue from Humans with Atrial Tissue from Humans with

Atrial FibrillationAtrial Fibrillation

Control(n=7)

10 µM(n=7)

APD20 (ms) 25 ± 4 34 ± 6**

APD90 (ms) 229 ± 13 243 ± 16**

ERP (ms) 239 ± 11 259 ± 11**

Resting potential (mV) -76 ± 1 -74 ± 1

dV/dtmax (V/s) 244 ± 38 219 ± 32

Page 7: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Fedida et al. J Cardiovasc Electrophysiol 2005Fedida et al. J Cardiovasc Electrophysiol 2005

Fedida. Curr Op Invest Drugs 2007Fedida. Curr Op Invest Drugs 2007

INa IC50 = 43 µM at -80 mV, 1 Hz

INa IC50 = 9 µM at -80 mV, 20 Hz

Vernakalant concentration (µM)

Fra

ctio

nal

cu

rren

t

1 10 100 10000.0

0.2

0.4

0.6

0.8

1.0

Plasma Levels in Patients

1 Hz

20 Hz

Vernakalant’s Frequency-Dependent Vernakalant’s Frequency-Dependent Block of Na Currents Targets AFBlock of Na Currents Targets AF

Page 8: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Slows Atrial Conduction Vernakalant Slows Atrial Conduction

at Fibrillatory Heart Rates in Dogsat Fibrillatory Heart Rates in Dogs

4 mg/kg4 mg/kg

****

**

0

20

40

60

80

100

200 240 300 400Pacing rates (beats/min)

% C

han

ge

in C

on

du

ctio

n T

ime

Nattel et al. European Society of Cardiology 2001Nattel et al. European Society of Cardiology 2001

Page 9: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Rapidly Converts Vernakalant Rapidly Converts Atrial Fibrillation in Dog ModelsAtrial Fibrillation in Dog Models

Frequency ofConversion

Time toConversion (min)

1 mg/kg 55% 10.0 ± 4.1

2 mg/kg 88% 6.9 ± 2.5

4 mg/kg 100% 5.1 ± 3.4

8 mg/kg 100% 2.8 ± 2.5

Vernakalant dose dependently decreased time to conversionVernakalant dose dependently decreased time to conversion

Nattel et al. European Society of Cardiology 2001Nattel et al. European Society of Cardiology 2001

Page 10: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Reduced Pro-arrhythmia in theReduced Pro-arrhythmia in thePig Acute MI ModelPig Acute MI Model

TreatmentIschemia

VT/VFReperfusion

VT/VFTotal

Mortality

Saline 4/7 2/3 6/7

Flecainide 9/9 – 9/9

Vernakalant 2/8 0/6 2/8*

* P<0.05 Fishers Exact Test, compared to saline and compared to flecainide* P<0.05 Fishers Exact Test, compared to saline and compared to flecainide

Page 11: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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10 min IV infusion (0, 2, 8, 16 mg/kg), 30 min dose increment; Results - mean ± sem (n = 6);10 min IV infusion (0, 2, 8, 16 mg/kg), 30 min dose increment; Results - mean ± sem (n = 6);

*Denotes statistical significance compared to vehicle control (P<0.05); [Qtest Study SPD06-004]*Denotes statistical significance compared to vehicle control (P<0.05); [Qtest Study SPD06-004]

0 5000 10000 15000 20000 250000

20

40

60

80

100

120

Cmax in patients

SystolicDiastolic

*

Cplasma (ng/mL)

Blo

od

Pre

ssu

re (

mm

Hg

)

At Therapeutic Concentrations, At Therapeutic Concentrations, Vernakalant has Little Effect on Blood Vernakalant has Little Effect on Blood

Pressure in the Anesthetized DogPressure in the Anesthetized Dog

Page 12: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Mechanism of ActionMechanism of Action

Greg Beatch, Ph.D.Greg Beatch, Ph.D.Vice President, Scientific AffairsVice President, Scientific Affairs

Cardiome Pharma Corp.Cardiome Pharma Corp.

Page 13: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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VernakalantVernakalantMechanism of ActionMechanism of Action

• Multiple ion channel blockerMultiple ion channel blocker– Targeted to AFTargeted to AF

• Relatively atrial selectiveRelatively atrial selective

• Rapid conversion of atrial fibrillationRapid conversion of atrial fibrillation

• Pharmacologic effects consistent with Pharmacologic effects consistent with ion channel blocking profileion channel blocking profile

Page 14: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Blocks K+ Channels Vernakalant Blocks K+ Channels Important in Atrial RepolarizationImportant in Atrial Repolarization

Current IC50 (µM)

Ito 5-30

IKur 3-13

IKACh 10

IKr 7-21

IKs > 100

IK1 > 1000 100 200 300 400 ms

IKur

IKr

Ito

IKACh

0 mV

Fedida et al. J Cardiovasc Electrophysiol 2005Fedida et al. J Cardiovasc Electrophysiol 2005

Page 15: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Effects of Vernakalant on Effects of Vernakalant on Atrial Tissue from Humans with Atrial Tissue from Humans with

Atrial FibrillationAtrial Fibrillation

Control(n=7)

10 µM(n=7)

APD20 (ms) 25 ± 4 34 ± 6**

APD90 (ms) 229 ± 13 243 ± 16**

ERP (ms) 239 ± 11 259 ± 11**

Resting potential (mV) -76 ± 1 -74 ± 1

dV/dtmax (V/s) 244 ± 38 219 ± 32

Ravens et al. European Society of Cardiology 2007Ravens et al. European Society of Cardiology 2007

Data collected at 60 bpm; ** P<0.01Data collected at 60 bpm; ** P<0.01

Page 16: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Prolongs Atrial Vernakalant Prolongs Atrial Refractory Period: Human EP StudyRefractory Period: Human EP Study

* P<0.05 vs. baseline* P<0.05 vs. baseline

Dorian et al. J Cardiovasc Pharmacol 2007Dorian et al. J Cardiovasc Pharmacol 20074 mg/kg4 mg/kg

100 bpm pacing100 bpm pacing

**

0

10

20

30

40

AERP VERP

Ch

ang

e fr

om

Bas

elin

e (m

sec)

Page 17: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Data collected at 60 bpm; ** P<0.01Data collected at 60 bpm; ** P<0.01

Ravens et al. European Society of Cardiology 2007Ravens et al. European Society of Cardiology 2007

Effects of Vernakalant on Effects of Vernakalant on Atrial Tissue from Humans with Atrial Tissue from Humans with

Atrial FibrillationAtrial Fibrillation

Control(n=7)

10 µM(n=7)

APD20 (ms) 25 ± 4 34 ± 6**

APD90 (ms) 229 ± 13 243 ± 16**

ERP (ms) 239 ± 11 259 ± 11**

Resting potential (mV) -76 ± 1 -74 ± 1

dV/dtmax (V/s) 244 ± 38 219 ± 32

Page 18: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Fedida et al. J Cardiovasc Electrophysiol 2005Fedida et al. J Cardiovasc Electrophysiol 2005

Fedida. Curr Op Invest Drugs 2007Fedida. Curr Op Invest Drugs 2007

INa IC50 = 43 µM at -80 mV, 1 Hz

INa IC50 = 9 µM at -80 mV, 20 Hz

Vernakalant concentration (µM)

Fra

ctio

nal

cu

rren

t

1 10 100 10000.0

0.2

0.4

0.6

0.8

1.0

Plasma Levels in Patients

1 Hz

20 Hz

Vernakalant’s Frequency-Dependent Vernakalant’s Frequency-Dependent Block of Na Currents Targets AFBlock of Na Currents Targets AF

Page 19: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Slows Atrial Conduction Vernakalant Slows Atrial Conduction

at Fibrillatory Heart Rates in Dogsat Fibrillatory Heart Rates in Dogs

4 mg/kg4 mg/kg

****

**

0

20

40

60

80

100

200 240 300 400Pacing rates (beats/min)

% C

han

ge

in C

on

du

ctio

n T

ime

Nattel et al. European Society of Cardiology 2001Nattel et al. European Society of Cardiology 2001

Page 20: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Rapidly Converts Vernakalant Rapidly Converts Atrial Fibrillation in Dog ModelsAtrial Fibrillation in Dog Models

Frequency ofConversion

Time toConversion (min)

1 mg/kg 55% 10.0 ± 4.1

2 mg/kg 88% 6.9 ± 2.5

4 mg/kg 100% 5.1 ± 3.4

8 mg/kg 100% 2.8 ± 2.5

Vernakalant dose dependently decreased time to conversionVernakalant dose dependently decreased time to conversion

Nattel et al. European Society of Cardiology 2001Nattel et al. European Society of Cardiology 2001

Page 21: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Reduced Pro-arrhythmia in theReduced Pro-arrhythmia in thePig Acute MI ModelPig Acute MI Model

TreatmentIschemia

VT/VFReperfusion

VT/VFTotal

Mortality

Saline 4/7 2/3 6/7

Flecainide 9/9 – 9/9

Vernakalant 2/8 0/6 2/8*

* P<0.05 Fishers Exact Test, compared to saline and compared to flecainide* P<0.05 Fishers Exact Test, compared to saline and compared to flecainide

Page 22: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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10 min IV infusion (0, 2, 8, 16 mg/kg), 30 min dose increment; Results - mean ± sem (n = 6);10 min IV infusion (0, 2, 8, 16 mg/kg), 30 min dose increment; Results - mean ± sem (n = 6);

*Denotes statistical significance compared to vehicle control (P<0.05); [Qtest Study SPD06-004]*Denotes statistical significance compared to vehicle control (P<0.05); [Qtest Study SPD06-004]

0 5000 10000 15000 20000 250000

20

40

60

80

100

120

Cmax in patients

SystolicDiastolic

*

Cplasma (ng/mL)

Blo

od

Pre

ssu

re (

mm

Hg

)

At Therapeutic Concentrations, At Therapeutic Concentrations, Vernakalant has Little Effect on Blood Vernakalant has Little Effect on Blood

Pressure in the Anesthetized DogPressure in the Anesthetized Dog

Page 23: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Effects on Purkinje Vernakalant Effects on Purkinje Fiber Action Potential DurationFiber Action Potential Duration

* P<0.05, ** P<0.01, ‡ P<0.005 vs. predrug* P<0.05, ** P<0.01, ‡ P<0.005 vs. predrug

Orth et al. Cardiovasc Res 2006Orth et al. Cardiovasc Res 2006

Drug Concentration (µM)

0.001 0.01 0.1 1 10 100

% C

han

ge

in a

ctio

n p

ote

nti

al d

ura

tio

n (

AP

D)

0

20

40

60

80

100

120

* **

****

*

**vernakalant

dofetilide

▲ APD50

APD90

**

**

Page 24: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Abolishes EADs in Vernakalant Abolishes EADs in Rabbit Purkinje FibersRabbit Purkinje Fibers

Orth et al. Cardiovasc Res 2006Orth et al. Cardiovasc Res 2006

3 s

300 nMdofetilide, 3 minEAD

Control: 60 beats/min

500 ms

0 mV

-80 mV-

3 s

300 nMdofetilide+ 30 µM vernakalant

0 mV

-80 mV-

EADs

300 nMdofetilide15 min

0 mV

-80 mV 3 s Stimartifact

-

Page 25: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Vernakalant Suppresses Vernakalant Suppresses Torsade de Pointes in vivoTorsade de Pointes in vivo

* P<0.05 Fishers Exact Test* P<0.05 Fishers Exact Test

Orth et al. Cardiovasc Res 2006Orth et al. Cardiovasc Res 2006

Clofilium-induced torsade de pointes was suppressed by Clofilium-induced torsade de pointes was suppressed by vernakalant in a rabbit modelvernakalant in a rabbit model

Inci

den

ce o

f T

dP

0.0

0.2

0.4

0.6

0.87/97/9 7/97/9

6/96/9

1/91/9*

ControlControl 0.10.1 0.30.3 11Dose of vernakalantDose of vernakalant

(µmol/kg/min)(µmol/kg/min)

*

Du

rati

on

of

Td

P (

s)

0.10.1 0.30.3 11Dose of vernakalantDose of vernakalant

(µmol/kg/min)(µmol/kg/min)

ControlControl

1501.0

Page 26: 1 Mechanism of Action Greg Beatch, Ph.D. Vice President, Scientific Affairs Cardiome Pharma Corp.

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Mechanism of ActionMechanism of ActionSummarySummary

• Multiple ion channel blockerMultiple ion channel blocker

• Activity potentiated in atria during AFActivity potentiated in atria during AF

• Converts AF rapidly and suppresses Converts AF rapidly and suppresses torsade de pointes in animal modelstorsade de pointes in animal models

• Pharmacologic effects consistent with Pharmacologic effects consistent with ion channel blocking profileion channel blocking profile