VELSIPITY

This brand name is authorized in Austria, Canada, Estonia, France, Croatia, Ireland, Italy, Lithuania, United States

Active ingredients

The drug VELSIPITY contains one active pharmaceutical ingredient (API):

1 Etrasimod
UNII 6WH8495MMH - ETRASIMOD

Etrasimod is a sphingosine-1-phosphate (S1P) receptor modulator that binds to S1P receptors 1, 4 and 5 (S1P1,4,5) and is a balanced G-protein and beta-arrestin agonist at S1P1. Etrasimod has minimal activity on S1P3 and no activity on S1P2. Etrasimod partially and reversibly blocks the capacity of lymphocytes to egress from lymphoid organs, reducing the number of lymphocytes in peripheral blood thereby lowering the number of activated lymphocytes in the tissue. The mechanism by which etrasimod exerts therapeutic effects in ulcerative colitis is unknown but may involve the reduction of lymphocyte migration into sites of inflammation.

Read about Etrasimod

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
VELSIPITY Film-coated tablet FDA, National Drug Code (US) MPI, US: SPL/PLR
VELSIPITY Film-coated tablet European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
L04AE05 L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AE Sphingosine-1-phosphate (S1P) receptor modulators
Discover more medicines within L04AE05

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02544903
Country: EE Ravimiamet Identifier(s): 3063585, 3063596, 3063608
Country: FR Base de données publique des médicaments Identifier(s): 62832598
Country: IT Agenzia del Farmaco Identifier(s): 051115018, 051115020, 051115032
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1099032, 1099033, 1099034
Country: US FDA, National Drug Code Identifier(s): 0069-0274, 63539-274

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