Skip to content
Surf Wiki
Save to docs
general/h1-receptor-antagonists

From Surf Wiki (app.surf) — the open knowledge base

Alcaftadine

Chemical compound


Chemical compound

FieldValue
Verifiedfieldschanged
Watchedfieldschanged
verifiedrevid477316420
imageAlcaftadine.svg
image_classskin-invert-image
tradenameLastacaft
Drugs.com
MedlinePlusa611022
DailyMedIDAlcaftadine
pregnancy_AU
routes_of_administrationEye drops
ATC_prefixS01
ATC_suffixGX11
legal_AU
legal_BR
legal_CA
legal_DE
legal_NZ
legal_UK
legal_USOTC
legal_US_comment
legal_UN
legal_status
elimination_half-life~2 hrs
CAS_number_Ref
CAS_number147084-10-4
PubChem19371515
IUPHAR_ligand7587
DrugBank_Ref
DrugBankDB06766
ChemSpiderID_Ref
ChemSpiderID14201635
UNII_Ref
UNII7Z8O94ECSX
KEGG_Ref
KEGGD06552
ChEBI_Ref
ChEBI71023
ChEMBL_Ref
ChEMBL1201747
IUPAC_name2-(1-Methylpiperidin-4-ylidene)-4,7-diazatricyclo[8.4.0.0(3,7)]tetradeca- 1(14),3,5,10,12-pentaene-6-carbaldehyde
C19H=21N=3O=1
SMILESCN1CCC(=C2c3ccccc3CCn4c(C=O)cnc24)CC1
StdInChI_Ref
StdInChI1S/C19H21N3O/c1-21-9-6-15(7-10-21)18-17-5-3-2-4-14(17)8-11-22-16(13-23)12-20-19(18)22/h2-5,12-13H,6-11H2,1H3
StdInChIKey_Ref
StdInChIKeyMWTBKTRZPHJQLH-UHFFFAOYSA-N

| Drugs.com =

| elimination_half-life = ~2 hrs

Alcaftadine, sold under the brand name Lastacaft, is an antihistamine used to help prevent itching of the eyes. It is an H1 histamine receptor antagonist. It is given as an drops in the eye.

It was approved for medical use in the United States in July 2010. It is available as a generic medication and as an over-the-counter medication.

Medical uses

Alcaftadine is indicated for the prevention of itching associated with allergic conjunctivitis.

Pharmacology

Alcaftadine is an antagonist of histamine receptor 1. By blocking the receptor, alcaftadine has been shown to reduce itching and redness of the eyes, and to reduce recruitment of eosinophils after exposure to an allergen. Alcaftadine reduces the number of eosinophils compared to olopatadine 0.1%, and in animal models, alcaftadine 0.25% decreased the expression of the epithelial protein E-cadhedrin-1 compared to placebo. Reducing E-cadherin decreases junctions that lead to the progression of allergic conjunctivitis.

Adverse effects

In studies comparing the effectiveness of olopatadine to alcaftadine, there was not a dose-response increase of adverse effects as alcaftadine doses increases for 0.05% to 0.1% to 0.25%. The most common seen side effect of alcaftadine administration was irritation or a stinging sensation at the administration site.

Pharmacokinetics

Because alcaftadine is administered at low concentrations and at a local site (the eye), it appears to have minimal systemic effects, and the low absorption of alcaftadine results in minimal systemic accumulation.

History

When alcaftadine was tested against placebo and olopatadine, only alcaftadine 0.25% showed a clinically significant reduction in conjunctival redness scores 7 and 15 minutes after administration. Alcaftadine 0.05%, 0.1%, and 0.25% all reduced lid swelling, conjunctival redness, and ocular itching/tearing compared to placebo.

Society and culture

Economics

Allergan, Inc. began selling alcaftadine under the trade name Lastacaft after it was approved by the US Food and Drug Administration in July 2010. By March 2012, 139,000 prescriptions had been written for 104,000 unique patients, and alcaftadine exceeded the sales of epinastine (Elestat).

Alcaftadine was approved for medical use in the United States in July 2010.

References

References

  1. (10 August 2022). "Lastacaft- alcaftadine solution/ drops".
  2. (24 December 1999). "Drug Approval Package: Lastacaft (alcaftadine) Ophthalmic Solution NDA #022134".
  3. (15 March 2022). "Now Available Over the Counter, Lastacaft Provides Eye Allergy Itch Relief in Minutes that Lasts Through 16 Hours".
  4. (1 August 2015). "Lastacaft- alcaftadine solution/ drops".
  5. (January 2011). "Evaluation of alcaftadine 0.25% ophthalmic solution in acute allergic conjunctivitis at 15 minutes and 16 hours after instillation versus placebo and olopatadine 0.1%". Clinical Ophthalmology.
  6. (February 2011). "Comparison of effects of alcaftadine and olopatadine on conjunctival epithelium and eosinophil recruitment in a murine model of allergic conjunctivitis". Drug Design, Development and Therapy.
  7. (28 November 2009). "Alcaftadine". U.S. Food and Drug Administration.
  8. (24 December 1999). "Drug Approval Package: Lastacaft (alcaftadine) Ophthalmic Solution NDA #022134".
  9. (21 June 2012). "Lastacaft (alcaftadine ophthalmic solution 0.25%)". U.S. [[Food and Drug Administration]] (FDA).
Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

Want to explore this topic further?

Ask Mako anything about Alcaftadine — get instant answers, deeper analysis, and related topics.

Research with Mako

Free with your Surf account

Content sourced from Wikipedia, available under CC BY-SA 4.0.

This content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.

Report