New Release: Alpha testing version has been released.

Lasmiditan

N02C - Antimigraine preparations ATC N02CC08 Small molecule approved 2020 Oral First-in-class

JFDA label: Acumig

Mechanism of Action

Agonist of 5-hydroxytryptamine receptor 1F — Serotonin 1f (5-HT1f) receptor agonist

TargetActionGene / class
5-hydroxytryptamine receptor 1F efficacy AGONIST HTR1F

Indications

Approved

  • Migraine Disorders — migraine disorder

Contraindications

Source: openFDA

  • None. None. ( 4 ) Absolute

Dosing

Source: openFDA

The recommended dose of REYVOW is 50 mg, 100 mg, or 200 mg taken orally, as needed. No more than one dose should be taken in 24 hours, and REYVOW should not be taken unless the patient can wait at least 8 hours between dosing and driving or operating machinery [see Warnings and Precautions ( 5.1 )] . A second dose of REYVOW has not been shown to be effective for the same migraine attack. The safety of treating an average of more than 4 migraine attacks in a 30-day period has not been established. REYVOW may be taken with or without food. Administer tablets whole; do not split, crush, or chew. The recommended dose is 50 mg, 100 mg, or 200 mg taken orally, as needed. ( 2 ) No more than one dose should be taken in 24 hours. ( 2 , 5.1 ) Administer tablets whole. ( 2 )

Warnings & Precautions

Source: openFDA

Warnings & Precautions

Driving Impairment: Advise patients not to drive or operate machinery until at least 8 hours after taking each dose of REYVOW. Patients who cannot follow this advice should not take REYVOW. Patients may not be able to assess their own driving competence and the degree of impairment caused by REYVOW. ( 5.1 ) Central Nervous System (CNS) Depression: REYVOW may cause CNS depression and should be used with caution if used in combination with alcohol or other CNS depressants. ( 5.2 , 7.1 ) Serotonin Syndrome: Reactions consistent with serotonin syndrome were reported in patients treated with REYVOW. Discontinue REYVOW if symptoms of serotonin syndrome occur. ( 5.3 ) Medication Overuse Headache: Detoxification may be necessary. ( 5.4 )

Driving Impairment REYVOW may cause significant driving impairment

Driving Impairment REYVOW may cause significant driving impairment. In a driving study, administration of single 50 mg, 100 mg, or 200 mg doses of REYVOW significantly impaired subjects' ability to drive [see Clinical Studies ( 14.2 )] . Additionally, more sleepiness was reported at 8 hours following a single dose of REYVOW compared to placebo. Advise patients not to engage in potentially hazardous activities requiring complete mental alertness, such as driving a motor vehicle or operating machinery, for at least 8 hours after each dose of REYVOW. Patients who cannot follow this advice should not take REYVOW. Prescribers and patients should be aware that patients may not be able to assess their own driving competence and the degree of impairment caused by REYVOW.

Central Nervous System Depression REYVOW may cause central nervous sys

Central Nervous System Depression REYVOW may cause central nervous system (CNS) depression, including dizziness and sedation [see Adverse Reactions ( 6.1 )] . Because of the potential for REYVOW to cause sedation, other cognitive and/or neuropsychiatric adverse reactions, and driving impairment, REYVOW should be used with caution if used in combination with alcohol or other CNS depressants [see Drug Interactions ( 7.1 )] . Patients should be warned against driving and other activities requiring complete mental alertness for at least 8 hours after REYVOW is taken [see Warnings and Precautions ( 5.1 )] .

Serotonin Syndrome In clinical trials, reactions consistent with serot

Serotonin Syndrome In clinical trials, reactions consistent with serotonin syndrome were reported in patients treated with REYVOW who were not taking any other drugs associated with serotonin syndrome. Serotonin syndrome may also occur with REYVOW during coadministration with serotonergic drugs [e.g., selective serotonin reuptake inhibitors (SSRIs), serotonin norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants (TCAs), and monoamine oxidase (MAO) inhibitors]. Serotonin syndrome symptoms may include mental status changes (e.g., agitation, hallucinations, coma), autonomic instability (e.g., tachycardia, labile blood pressure, hyperthermia), neuromuscular signs (e.g., hyperreflexia, incoordination), and/or gastrointestinal signs and symptoms (e.g., nausea, vomiting, diarrhea). The onset of symptoms usually occurs within minutes to hours of receiving a new or a greater dose of a serotonergic medication. Discontinue REYVOW if serotonin syndrome is suspected.

Medication Overuse Headache Overuse of acute migraine drugs (e.g., erg

Medication Overuse Headache Overuse of acute migraine drugs (e.g., ergotamines, triptans, opioids, or a combination of these drugs for 10 or more days per month) may lead to exacerbation of headache (i.e., medication overuse headache). Medication overuse headache may present as migraine-like daily headaches or as a marked increase in frequency of migraine attacks. Detoxification of patients including withdrawal of the overused drugs and treatment of withdrawal symptoms (which often includes a transient worsening of headache) may be necessary.

Pregnancy & Lactation

Lactation

Compatible Hale L1

If lasmiditan is required by the mother of an older infant, it is not a reason to discontinue breastfeeding, but until more data become available, an alternate drug may be preferred, especially while nursing a newborn or preterm infant.

Chemistry & Properties

2D structure
FormulaC19H18F3N3O2
Molecular weight377.37 g/mol
IUPAC name2,4,6-trifluoro-N-[6-(1-methylpiperidine-4-carbonyl)-2-pyridinyl]benzamide
CAS439239-90-4
PubChem CID11610526
InChIKeyXEDHVZKDSYZQBF-UHFFFAOYSA-N
logP3.28 (XLogP 2.8)
Polar surface area62.3 Ų
H-bond acceptors / donors4 / 1
Drug-likeness (QED)0.83
Lipinski violations0
SMILESCN1CCC(C(=O)c2cccc(NC(=O)c3c(F)cc(F)cc3F)n2)CC1

Biology & Pharmacokinetics

Pharmacokinetics predicted

Bioavailability10.0%
Half-life2.194 h
Volume of distribution2.77 L/kg
Protein binding72.8%
BBB penetrantYes

Enzyme interactions

EnzymeRoleDetail
CYP3A4Substrate

Receptor binding (top 1)

TargetActionAffinity
5-HT1F receptor (HTR1F) Agonist pKi 8.7

Transporters

BCRP (Inhibitor)BSEP (Inhibitor)MATE1 (Inhibitor)MRP1 (Inhibitor)OATP1B1 (Inhibitor)OATP1B3 (Inhibitor)OCT1 (Inhibitor)P-gp (Inhibitor)P-gp (Substrate)

Drug–drug interactions (100+, DDInter)

Interacting drugSeverityManagement
Dexfenfluramine major
Dextromethorphan major
Dolasetron major
Doxepin major
Doxepin (topical) major
Edoxaban major
Fenfluramine major
Granisetron major
Lorcaserin major
Methylene blue major
Ondansetron major
Ozanimod major
Palonosetron major
Procarbazine major
Sibutramine major
Siponimod major
Acrivastine moderate
Afatinib moderate
Aldesleukin moderate
Alectinib moderate
Alimemazine moderate
Alpelisib moderate
Apixaban moderate
Apremilast moderate
Artesunate moderate
Atropine moderate
Azatadine moderate
Azelastine (nasal) moderate
Belinostat moderate
Betrixaban moderate
Bosutinib moderate
Brentuximab vedotin moderate
Brompheniramine moderate
Bupropion moderate
Cabazitaxel moderate
Carbinoxamine moderate
Ceritinib moderate
Cetirizine moderate
Chlorcyclizine moderate
Chlorphenesin moderate

Showing 40 of 100+.

Registered Products (4)

BrandForm / strengthPackAgentCitizen (JOD)
Acumig Tablet 50 mg 4 tab pack varies Hikma Pharmaceuticals Co.Ltd/Jordan 10.810
Acumig Tablet 100 mg 4 tab pack varies Hikma Pharmaceuticals Co.Ltd/Jordan 18.630
Acumig Tablet 50 mg 8 tab pack varies Hikma Pharmaceuticals Co.Ltd/Jordan 21.640
Acumig Tablet 100 mg 8 tab pack varies Hikma Pharmaceuticals Co.Ltd/Jordan 35.490