List of Suppliers' Lubricants Glidants Excipients Application used in Lacosamide on PharmaCompass.com

Aptra Synthesis Lacosamide

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Metrochem Lacosamide

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xyz-pharma-m-2024-09-09

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Shandong Loncom Pharmaceutical Lacosamide

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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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xyz-pharma-m-2024-09-09

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CHEMISTRY
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ACTIVE PHARMA INGREDIENTS

70 API Suppliers, 31 USDMF, 22 CEP/COS, 5 JDMF, 22 EU WC, 10 KDMF, 21 NDC API, 41 Listed Suppliers, $ API Reference Price

70 API Suppliers
31 USDMF
22 CEP/COS
5 JDMF
22 EU WC
10 KDMF
21 NDC API
41 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

9 Drugs in Development

9 Drugs in Development

INTERMEDIATES

11 Intermediates Suppliers

11 Intermediates Suppliers

FINISHED DOSAGE FORMULATIONS

489 FDF Dossiers, 101 FDA Orange Book, 176 Europe, 46 Canada, 125 Australia, 4 South Africa, 37 Listed Dossiers

489 FDF Dossiers
101 FDA Orange Book
176 Europe
46 Canada
125 Australia
4 South Africa
37 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - 100MG, TABLET;ORAL - 150MG, TABLET;ORAL - 200MG, TABLET;ORAL - 50MG

drugProductComposition
TABLET;ORAL - 100MG
TABLET;ORAL - 150MG
TABLET;ORAL - 200MG
TABLET;ORAL - 50MG

RELATED EXCIPIENT COMPANIES

4 Rochem International Inc, 3 SPI Pharma, 2 Seqens, 5 DKSH, 8 Gangwal Healthcare, 3 Nanjing Well Pharmaceutical, 1 ACG Worldwide, 8 Actylis, 1 Aeon Procare, 5 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 10 BASF, 10 Corel Pharma Chem, 2 DFE Pharma, 2 Finar, 7 Gangwal Chemicals, 7 Ideal Cures Pvt Ltd, 17 Kerry, 4 Kima Chemical, 6 Lonza Capsugel, 11 Microlex e.U, 2 Nomisma Healthcare, 2 Novo Excipients, 1 Pharmatrans-Sanaq, 2 Pluviaendo, 2 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 1 Qualicaps, 18 Roquette, 6 Seppic, 3 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shijiazhuang Huaxu Pharmaceutical, 9 Sigachi Industries, 3 The Dow Chemical Company, 1 Valens Pharmachem, 2 Vasa Pharmachem, 1 Zhejiang Huakang Pharmaceutical

EXCIPIENTS BY APPLICATIONS

53 Coating Systems & Additives, 30 Fillers, Diluents & Binders, 28 Controlled & Modified Release, 22 Thickeners and Stabilizers, 18 Film Formers & Plasticizers, 15 Direct Compression, 13 Parenteral, 13 Lubricants & Glidants, 12 Topical, 11 Taste Masking, 11 Solubilizers, 9 Co-Processed Excipients, 9 Disintegrants & Superdisintegrants, 8 Granulation, 6 Chewable & Orodispersible Aids, 6 Emulsifying Agents, 5 Empty Capsules, 5 API Stability Enhancers, 5 Coloring Agents, 5 Rheology Modifiers, 4 Vegetarian Capsules, 1 Soft Gelatin

DIGITAL CONTENT

2 DATA COMPILATION #PharmaFlow, 72 NEWS #PharmaBuzz

media
2 DATA COMPILATION #PharmaFlow
72 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

168 Finished Drug Prices, 11 Annual Reports

globalSalesInformation
168 Finished Drug Prices
11 Annual Reports

MARKET PLACE

18 APIs, 6 FDF Dossiers

marketPlace
18 APIs
6 FDF Dossiers

PATENTS & EXCLUSIVITIES

18 US Patents, 12 US Exclusivities, 10 Health Canada Patents

patents
18 US Patents
12 US Exclusivities
10 Health Canada Patents

REF. STANDARDS & IMPURITIES

7 Others

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7 Others

Aptra Synthesis Lacosamide

Synopsis

ACTIVE PHARMA INGREDIENTS

70

API Suppliers

31

USDMF

22

CEP/COS

CEP/COS Certifications

5

JDMF

22

EU WC

10

KDMF

21

NDC API

0

VMF

41

Listed Suppliers

API REF. PRICE (USD/KG)

$

$ 531

MARKET PLACE

18

API

6

FDF

11INTERMEDIATES

FINISHED DOSAGE FORMULATIONS

489

FDF Dossiers

101

FDA Orange Book

FDA (Orange Book)

176

Europe

46

Canada

125

Australia

4

South Africa

37

Listed Dossiers

9DRUGS IN DEVELOPMENT

DRUG PRODUCT COMPOSITIONS

REF. STANDARDS OR IMPURITIES

0

EDQM

0

USP

0

JP

7

Others

PATENTS & EXCLUSIVITIES

18

US Patents

12

US Exclusivities

10

Health Canada Patents

DIGITAL CONTENT

2

Data Compilation #PharmaFlow

0

Stock Recap #PipelineProspector

0

Weekly News Recap #Phispers

72

News #PharmaBuzz

GLOBAL SALES INFORMATION

US Medicaid (USD)

NA

Annual Reports (USD Million)

8,467

Finished Drug Prices

171 RELATED EXCIPIENT COMPANIES

289EXCIPIENTS BY APPLICATIONS

Chemistry

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Also known as: 175481-36-4, Erlosamide, Vimpat, (r)-2-acetamido-n-benzyl-3-methoxypropanamide, Harkoseride, Spm 927

Molecular Formula

C₁₃H₁₈N₂O₃

Molecular Weight

250.29 g/mol

InChI Key

VPPJLAIAVCUEMN-GFCCVEGCSA-N

FDA UNII

563KS2PQY5

Lacosamide

Lacosamide is a functionalized amino acid compound specifically synthesized as an anticonvulsive drug to use as add-on therapy for partial-onset seizures with antinociceptive and neuroprotective activities. Lacosamide selectively enhances slow inactivation of voltage-gated sodium channels without affecting fast inactivation, thereby stabilizing hyperexcitabe neuronal membranes. Furthermore, this agent binds to collapsin response mediator protein 2 (CRMP2; DPYSL2), a cytosolic phosphoprotein expressed in most tissues. In the nervous system, CRMP2 acts as a mediator of growth cone collapse as well as modifies axon number, length, and neuronal polarity.

The physiologic effect of lacosamide is by means of Decreased Central Nervous System Disorganized Electrical Activity.

1 2D Structure

Lacosamide

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

(2R)-2-acetamido-N-benzyl-3-methoxypropanamide

2.1.2 InChI

InChI=1S/C13H18N2O3/c1-10(16)15-12(9-18-2)13(17)14-8-11-6-4-3-5-7-11/h3-7,12H,8-9H2,1-2H3,(H,14,17)(H,15,16)/t12-/m1/s1

2.1.3 InChI Key

VPPJLAIAVCUEMN-GFCCVEGCSA-N

2.1.4 Canonical SMILES

CC(=O)NC(COC)C(=O)NCC1=CC=CC=C1

2.1.5 Isomeric SMILES

CC(=O)N[C@H](COC)C(=O)NCC1=CC=CC=C1

2.2 Other Identifiers

2.2.1 UNII

563KS2PQY5

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 2-(acetylamino)-3-methoxy-n-(phenylmethyl)-, (2r)-

2. Add-234037

3. Ertosamide

4. Harkoseride

5. Spm-927

2.3.2 Depositor-Supplied Synonyms

1. 175481-36-4

2. Erlosamide

3. Vimpat

4. (r)-2-acetamido-n-benzyl-3-methoxypropanamide

5. Harkoseride

6. Spm 927

7. Spm-927

8. (2r)-2-acetamido-n-benzyl-3-methoxypropanamide

9. (r)-lacosamide 1

10. Propanamide, 2-(acetylamino)-3-methoxy-n-(phenylmethyl)-, (2r)-

11. Add 243037

12. Add-234037

13. Chembl58323

14. 563ks2pqy5

15. Add-243037

16. Erlosamide [inn]

17. Ncgc00253740-01

18. (r)-2-acetamido-n-benzyl-3-methoxypropionamide.

19. (r)-2-acetylamino-n-benzyl-3-methoxy-propionamide

20. Lacosamide [usan]

21. (+)-(2r)-2-(acetylamino)-n-benzyl-3-methoxypropanamide

22. Ertosamide

23. Add 234037

24. Harkeroside

25. Unii-563ks2pqy5

26. Lacosamide [usan:inn:ban]

27. Lacosamide Cv

28. Spm-929

29. Lacosamide Racemate

30. Lacosamide- Bio-x

31. (2r)-2-(acetylamino)-n-benzyl-3-methoxypropanamide

32. Vimpat (tn)

33. Lacosamide [mi]

34. Lacosamide [inn]

35. Lacosamide [jan]

36. Lacosamide [vandf]

37. Lacosamide [mart.]

38. (r)-n-benzyl-2-acetamido-3-methoxypropionamide

39. Dsstox_cid_31455

40. Dsstox_rid_97341

41. Lacosamide [who-dd]

42. Dsstox_gsid_57666

43. Schembl35330

44. Lacosamide (jan/usan/inn)

45. Lacosamide [ema Epar]

46. Gtpl7472

47. Zinc7673

48. Dea No. 2746

49. Lacosamide Cv [usp-rs]

50. Dtxsid1057666

51. Lacosamide [orange Book]

52. Lacosamide [ep Monograph]

53. Chebi:135939

54. Lacosamide [usp Monograph]

55. Bcp02197

56. Tox21_113857

57. Bdbm50300204

58. Mfcd08272557

59. Akos005146274

60. Lacosamide 1.0 Mg/ml In Acetonitrile

61. Cs-0529

62. Db06218

63. Ks-1227

64. Ac-22750

65. Am808141

66. Bl164605

67. Hy-13015

68. A3897

69. Bb 0260890

70. Cas-175481-36-4

71. (r)-n-benzyl-2-acetamido-3-methoxypropanamide

72. D07299

73. (2r)-n-benzyl-2-acetamido-3-methoxypropanamide

74. (r)-2-acetamido-n-benzyl-3-methoxypropionamide

75. (r)-n-benzyl 2-acetamido-3-methoxypropionamide

76. (r)-n-benzyl 2-acetamido-3-methoxypropionamide,

77. Ab01559947-01

78. (2r)-2-acetylamino-n-benzyl-3-methoxypropanamide

79. (r)-2-acetylamino-n-benzyl-3-methoxypropionamide

80. 481l364

81. Ar-270/11402703

82. Q420077

83. Sr-01000942286

84. Sr-01000942286-1

85. (2r)-2-acetamido-3-methoxy-n-(phenylmethyl)propanamide

86. 2-(acetylamino)-3-methoxy-n-(phenylmethyl)-, (2r)-

87. Z1550648754

88. Lacosamide Solution, 1.0 Mg/ml In Acetonitrile, Ampule Of 1 Ml, Certified Reference Material

2.4 Create Date

2005-08-09

3 Chemical and Physical Properties

Molecular Formula	C₁₃H₁₈N₂O₃
Molecular Weight	250.29 g/mol
XLogP3	0.3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	6
Exact Mass	250.13174244 g/mol
Monoisotopic Mass	250.13174244 g/mol
Topological Polar Surface Area	67.4 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	275
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

4 Drug and Medication Information

4.1 Drug Information

1 of 2
Drug Name	Vimpat
PubMed Health	Lacosamide
Drug Classes	Anticonvulsant
Active Ingredient	Lacosamide
Dosage Form	Tablet; Solution
Route	Oral; Intravenous
Strength	200mg/20ml (10mg/ml); 200mg; 150mg; 10mg/ml; 100mg; 50mg
Market Status	Prescription
Company	Ucb

2 of 2
Drug Name	Vimpat
PubMed Health	Lacosamide
Drug Classes	Anticonvulsant
Active Ingredient	Lacosamide
Dosage Form	Tablet; Solution
Route	Oral; Intravenous
Strength	200mg/20ml (10mg/ml); 200mg; 150mg; 10mg/ml; 100mg; 50mg
Market Status	Prescription
Company	Ucb

4.2 Drug Indication

Lacosamide is indicated for adjunctive therapy for partial onset seizures in patients with epilepsy over 17 years old. Injection is indicated for short term use when oral therapy is not feasible.

FDA Label

Vimpat is indicated as monotherapy and adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy.

Lacosamide Accord is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy.

Lacosamide Accord is indicated as adjunctive therapy

in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy.

in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Lacosamide UCB is indicated as monotherapy and adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy.

Treatment of epilepsy with partial-onset seizures

Treatment of generalised epilepsy and epileptic syndromes

5 Pharmacology and Biochemistry

5.1 Pharmacology

Lacosamide therapy is correlated with a decrease in seizure frequency. It should be noted that in group analyses, dosages above 400 mg/day do not appear to result in additional benefit.

5.2 FDA Pharmacological Classification

5.2.1 Active Moiety

LACOSAMIDE

5.2.2 FDA UNII

563KS2PQY5

5.2.3 Pharmacological Classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]; Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

5.3 ATC Code

N03AX18

N03AX18

N03AX18

N03AX18

S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355

N - Nervous system

N03 - Antiepileptics

N03A - Antiepileptics

N03AX - Other antiepileptics

N03AX18 - Lacosamide

5.4 Absorption, Distribution and Excretion

Absorption

Lacosamide has a negligible first pass effect with bioavailability of about 100%. The maximum Lacosamide plasma concentrations occur about 1-4 hours after oral administration, and the pharmacokinetics of Lacosamide are dose proportional. Food does not affect absorption.

Route of Elimination

Lacosamide is eliminated primarily from the systemic circulation by biotransformation and renal excretion.

Volume of Distribution

approximately 0.6 L/kg; thus close to the volume of total body water.

Clearance

95% recovered in the urine 0.5% in the feces

5.5 Metabolism/Metabolites

Lacosamide is a CYP2C19 substrate. The relative contribution of other CYP isoforms or non-CYP enzymes in the metabolism of lacosamide is not known. Primary compounds excreted were unchanged lacosamide (approximately 40% of the dose), its O-desmethyl metabolite (approximately 30%), and a structurally unknown polar fraction (~20%). The plasma exposure of the major human metabolite, O-desmethyl-lacosamide, is approximately 10% of that of lacosamide. This metabolite has no known pharmacological activity.

5.6 Biological Half-Life

13 Hours

5.7 Mechanism of Action

It is proposed that lacosamide's inhibition of sodium channels is responsible for analgesia. Lacosamide may be selective for inhibiting depolarized neurons rather than neurons with normal resting potentials. Pain and nociceptor hyperexcitability are associated with neural membrane depolarization. Lacosamide binds to collapsin response mediator protein-2 (CRMP-2), a phosphoprotein which is expressed primarily in the nervous system and is involved in neuronal differentiation and control of axonal outgrowth. The role CRMP-2 of binding in seizure control is hasn't been elucidated.

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Number of Transactions

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Total Value (USD)

Quantity (KGS) & Unit rate (USD/KGS) over time

API Imports and Exports

Importing Country	Total Quantity (KGS)	Average Price (USD/KGS)	Number of Transactions

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DOSAGE - TABLET;ORAL - 100MG

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