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Newer Anticonvulsants: Targets and Toxicity Laura Tormoehlen, MD Neurology and EM-Toxicology

Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

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Page 1: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Newer Anticonvulsants: Targets and Toxicity

Laura Tormoehlen, MDNeurology and EM-Toxicology

Page 2: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Disclosures• No financial disclosures

Page 3: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

DEFINITIONS

Presenter
Presentation Notes
New= during or after my residency Third generation = 2005 and after Grouped not by year but by mechanism Tormoehlen not an epileptologist Anticonvulsants, not antiepileptics
Page 4: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Objectives/Outline• Mechanism of Action• Specific Indications• Toxicity• Adverse Effects

Page 5: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

LACOSAMIDE

Presenter
Presentation Notes
New= during or after my residency Tormoehlen not an epileptologist Anticonvulsants, not antiepileptics
Page 6: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Lacosamide• Trade Names: Vimpat• Dosage Forms: Oral, Intravenous• Mechanism of Action: Functionalized Amino Acid, decreases

hyperexcitability via:– Enhancing slow inactivation of voltage-gated sodium channels– CRMP-2 binding

• Indication:– Partial seizure, monotherapy– Partial seizure, adjunct

Presenter
Presentation Notes
“CRMP-2 is part of signal transduction cascade of neurotropic factors” Micromedex Signal protein involved in neuronal differentiation and growth
Page 7: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Lacosamide : Targets

Beyreuther BK, et al. Lacosamide: A Review of Preclinical Properties. CNS Drug Reviews 2001: 13(1): 21-42

Presenter
Presentation Notes
Time to peak concentration: 1-4 hours, Bioavailability: 100%, Protein Binding: less than 15%, Metabolites: inactive, Elimination: renal excretion, Half life: 13 hours, Hemodialysis: 50% removed by 4 hour session
Page 8: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Lacosamide : Toxicity• Cardiac Arrest

– 1 Fatal (Malissin 2013, PMID 23534387)

• Ingestion of 7 grams of lacosamide• Co-ingestion with lamotrigine, phenobarbital, and carbamazepine, plus• Initial rhythm asystole, resuscitated, followed by shock and multi-organ failure

– 1 Survival (Chua-Tuan 2015, PMID 25951877)

• Ingestion of 4.5 grams of lacosamide• Co-ingestion of cyclobenzaprine and levetiracetam• Initial rhythm pulseless ventricular tachycardia

• Coma and Seizures (Bauer 2008, PMID 20171144)

– Ingestion of 12 grams of lacosamide– Co-ingestion with gabapentin (56g), topiramate (2g), zonisamide (2.8g)– Also had PR prolongation (265 ms) and hypotension (60/30 mmHg)

Presenter
Presentation Notes
Plus = gabapentin, clonazepam, atorvastatin, amlodipine, valsartan Authors suspected drug-drug interaction of LCM with LMT and CBZ, among other things Also, one case report (Jones) of VPA toxicity (hyperammonemia and BM suppression) that started after LCM initiation – mechanism not clear
Page 9: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Lacosamide : Adverse Effects• Common: Nausea/Vomiting, Somnolence, Memory

Impairment, Dizziness/Vertigo, Headache, Diplopia, Ataxia, Tremor

• Worse with other VGSC blocking agents• Serious

• CV – Atrial fibrillation/flutter, PR interval prolongation, all degrees of AV block, bradycardia, syncope

• Immune – Drug hypersensitivity• Psych – Suicidal thoughts/behavior, Depression, Hallucinations

Presenter
Presentation Notes
Single case report of pancreatitis Case series (Novy) of 39 patients with neurotoxicity after addition of LCM to another VGSC blocker, 7 of those (18%) occurred without any changes to serum levels of the original drug Suspected pharamcodynamic interaction. Perhaps slow inactivated VGSCs (via LCM) are more susceptible to traditional drugs in this class. Sx improved after dose of first drug lowered. Perhaps because previous binding rate was restored. One case report of hepatotoxicity (Sunwoo) – AST 635, ALT 697
Page 10: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

LACOSAMIDEAnother Parenteral Sodium Channel Blocker

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RUFINAMIDE

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Rufinamide• Trade Names: Banzel• Dosage Forms: Oral• Mechanism of Action: Triazole Derivative

– Prolongs inactive state of sodium channels

• Indication:– Lennox-Gastaut syndrome, seizure, adjunct– Off Label: Partial seizure, adjunct

Page 13: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Rufinamide : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
Bioavailability: 85%, Tmax: 4-6 hours, Protein binding: 34%, Liver metabolism, renal excretion, Dialyzable: 29% removed, Half-life 6-10 hours No effect on GABA
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Rufinamide : Toxicity• An adult received 7200 mg during a clinical

trial without any adverse effects

Presenter
Presentation Notes
Usual dose 400-800 mg
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Rufinamide : Adverse Effects• Common: Nausea/Vomiting, Somnolence, Dizziness,

Headache, Diplopia/Blurred Vision, Ataxia/Gait Disturbance, Shortened QT Interval

• Serious:– Neurologic – Status Epilepticus– Psychiatric – Suicidal behavior– Hematologic – Leukopenia– Immune – Drug hypersensitivity syndrome/DRESS, Stevens-Johnson

syndrome

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RUFINAMIDEYet Another Sodium Channel Blocker, for Lennox-Gastaut

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ESLICARBAZEPINE

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Eslicarbazepine• Trade Names: Aptiom• Dosage Forms: Oral• Mechanism of Action: Structurally related to

carbamazepine and oxcarbazepine– Inhibition of voltage-gated sodium channels

• Indication:– Partial seizure, monotherapy– Partial seizure, adjuct

Page 19: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Johannessen-Landmark C and Johannessen SI. Modifications of Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21-39

Presenter
Presentation Notes
Reportedly has better side-effect profile than CBZ and OXC Anecdotally, not a big difference so far
Page 20: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Eslicarbazepine : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
Tmax 1-4 hours, Bioavailability: “highly”, Protein binding: less than 40%, Minor active metabolites (R-licarbazepine and oxcarbazepines), Hepatic glucuronidation, CYP 2C19 inhibitor, CYP 3A4 inducer, Partially dialyzable, Renal excretion, Half life: 13-20 hours
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Eslicarbazepine : Toxicity• Oxcarbazepine

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Eslicarbazepine : Adverse Effects• Common: Nausea/Vomiting, Somnolence, Dizziness,

Headache, Diplopia/Blurred Vision, Ataxia, Tremor• Serious:

– Psychiatric – Suicidal thoughts– Ophthalmologic – Visual impairment– Metabolic – Hyponatremia– Hematologic – Eosinophilia– Hepatic – Increased transaminases, Increased bilirubin– Immune – Anaphylaxis, Drug hypersensitivity syndrome/DRESS,

Stevens-Johnson syndrome– Other – Angioedema

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ESLICARBAZEPINEA Once-A-Day Oxcarbazepine

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PERAMPANEL

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Perampanel• Trade Names: Fycompa• Dosage Forms: Oral• Mechanism of Action: Noncompetetive antagonism

of AMPA receptors• Indication:

– Partial seizure, adjunct– Tonic-clonic seizure, adjunct– Orphan drug status for Lennox-Gastaut

Presenter
Presentation Notes
Initially studied for PD
Page 26: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Perampanel : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
Tmax: 0.5-2.5 hours, Protein binding: 95% -- very high, Extensive liver metabolism, Fecal and Renal excretion, Half life: 105 hours
Page 27: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Perampanel : Toxicity– Case report: 34 year-old with tuberous

sclerosis (Hoppner 2013, PMID 24001596)

• Ingestion of 204 mg, initially estimated to be 264 mg

• Dysarthria and fatigue, followed by stupor, then misperception and disorientation

• Impaired consciousness lasted 2 days• EEG without epileptiform discharges

Page 28: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Perampanel : Adverse Effects• Common: Somnolence, Dizziness, Headache,

Ataxia/Abnormal Gait/Falls, Dysarthria, Irritability, Mood Disorder

• Serious: – Psychiatric – Aggressive behavior, Homicidal

thoughts, Suicidal thoughts– Dermatologic – Drug hypersensitivity syndrome

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PERAMPANELAMPA antagonist, limited use due to SI/HI

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CLOBAZAM

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Clobazam• Trade Names: Onfi• Dosage Forms: Oral• Mechanism of Action: Benzodiazepine

– Binds to benzodiazepine site of GABA(A) and potentiate neurotransmission

• Indication:– Lennox-Gastaut, seizure, adjunct– Off Label: SGE, Partial seizure, adjunct– Not labeled for EtOH withdrawal or anxiety

Presenter
Presentation Notes
New in US, Old internationally
Page 32: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Clobazam : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
Tmax 0.5-4 hours, Bioavailability: 87%, Protein binding: 80-90% -- very high, Hepatic metabolism CYP 3A4, Active metabolite norclobazam, Induces 3A4, inhibits 2D6, Renal excretion 82%, Half life 26-42 hours, norclobazam 71-82 hours
Page 33: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Clobazam : Toxicity• It’s a Benzodiazepine

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Clobazam : Adverse Effects• Common: Somnolence/Sedation, Ataxia,

Dysarthria, Cough, Fever, Dependence, Constipation, Drooling, Insomnia

• Serious:– Dermatologic – Stevens-Johnson Syndrome, Toxic

Epidermal Necrolysis– Psychiatric – Suicidal Behavior/Ideation,

Aggressive Behavior

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CLOBAZAM“Less Sedating” Benzodiazepine

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VIGABATRIN

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Vigabatrin• Trade names: Sabril• Dosage Forms: Oral• Mechanism of Action:

– Irreversibly inhibits GABA Transaminase– May also stimulate GABA release

• Indication:– Partial seizure, adjunct– Infantile spasms– Restricted distribution, black box warning for vision loss

Page 38: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Vigabatrin : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
Bioavailability 50%, Protein binding: none, Hepatic metabolism, Renal excretion unchanged 95%, Dialyzable 40-60% removed, Half life 10 hours
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Vigabatrin : Toxicity• Case reports

– Adult ingested 8-12 grams• Psychosis

– 25 year-old woman ingested 60 grams• Severe delirium

Davie MB, Cook MJ, Ng C. Vigabatrin Overdose. Med J Aust 1996; 165: 403.

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Vigabatrin : Adverse Effects• Common: Somnolence, Dizziness/Vertigo,

Headache, Agitation• Serious:

– Ophthalmologic: Permanent vision loss– Neurologic: Coma, Seizures– Psychologic: Psychosis– Respiratory: Respiratory depression– Cardiovascular: Hypotension, Bradycardia

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VIGABATRINNovel agent, VERY limited use due to visual impairment

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EZOGABINE/RETIGABINE

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Ezogabine• Trade names: Potiga (US), Trobalt (Europe)• Dosage Forms: Oral• Mechanism of Action: Opens voltage-gated potassium

channels (KCNQ2/3) resulting in hyperpolarization• Indication:

– Partial seizure, in patients with inadequate response to several alternatives, adjunct

– Benign familial neonatal convulsions (loss of function of KCNQ2/3)– Black box warning for retinopathy

Page 44: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Ezogabine : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
KCNQ (Kv7.2 to 7.5) ion channels, activates and opens channels, stabilizes resting membrane potential --- lower bioavailability than the others Tmax: 0.5-2 hours
Page 45: Newer Anticonvulsants: Targets and Toxicity...Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21- 39 Reportedly has better side-effect profile

Ezogabine : Toxicity– Moderate: agitation, aggressive behavior,

irritability (doses greater than 2500 mg)– Severe:

• Cardiac dysrhythmias (asystole or ventricular tachycardia) within 3 hours of single 900-mg dose in 2 volunteers.

• QT prolongation known, TdP possible but not yet reported

Product Information: Potiga ® oral tablets, ezogabine oral tablets. GlaxoSmithKline (per FDA), Research Triangle Park, NC, 2015

Presenter
Presentation Notes
Clinical trials data Therapeutic dose: 600-1200mg daily, divided dose TID
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Ezogabine : Adverse Effects• Common: Fatigue, Memory Impairment, Vertigo,

Diplopia/Blurred Vision, Tremor, Incoordination/Abnormal gait, Aphasia/Dysarthria

• Serious:– Neurologic – Dizziness, Somnolence, Confusion– Ophthalmologic – Retinal disorder, Pigment change– Psychiatric – Hallucinations/Psychosis, Suicidal thoughts– Cardiovascular – Prolonged QT interval– Renal – Urinary retention– Dermatologic – Skin pigmentation (blue, grey, brown)

Presenter
Presentation Notes
Retinal change- 1/3 of patients after 4 years of use – visual monitoring every 6 months
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Zaugg BE, et al. Ezogabine maculopathy. Retinal Cases & Brief Reports 2016; 0: 1-6.

Presenter
Presentation Notes
Fundus photographs (A/B), then infrared images (C/D) at presentation (10 months of therapy), 6 months, and 12 months
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EZOGABINE“Niche drug,” limited use due to retinal/skin pigment changes and urinary retention

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GANAXOLONE

Presenter
Presentation Notes
Trial phase
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Johannessen-Landmark C and Johannessen SI. Modifications of Antiepileptic Drugs for Improved Tolerability and Efficacy. Perspect Med Chem 2008; 2: 21-39

Presenter
Presentation Notes
Neuroactive progesterone analogue, Positive modulator of GABA receptors, Trial phase
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Ganaxolone : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
Allosterically modulates the GABA-A receptor complex, lacks hormonal activity, Demonstrated efficacy in infantile spasms in children and monotherapy in adults
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SIRIPENTOL

Presenter
Presentation Notes
Available in Canada
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Stiripentol : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
Available in Canada
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BRIVARACETAM

Presenter
Presentation Notes
Should be available in US in Q2 2016
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Brivaracetam : Targets

Johannessen-Landmark C and Johannessen SI. Pharmacological Management of Epilepsy. Drugs 2008; 68(14): 1925-39.

Presenter
Presentation Notes
More potent binding to SV2a than levetiracetam, May also inhibit sodium channels, May have less psychiatric effects, Available Q2 2016
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QUESTIONS?

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