Wednesday, July 8, 2026

Drug profile · INN

fingolimod lauryl sulfate

fingolimod lauryl sulfate (TASCENSO ODT) is a sphingosine 1-phosphate receptor binding agent. Associated with BICYCLE THERAPEUTICS. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 20
Pipeline programs 0
News articles 0
Drug details — fingolimod lauryl sulfate
US status
approved
Class
Route
ORAL
Patents
20
Programs
0
Data quality
0.89

Quick answer

fingolimod lauryl sulfate (TASCENSO ODT) is a sphingosine 1-phosphate receptor binding agent. Associated with BICYCLE THERAPEUTICS. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN fingolimod lauryl sulfate
Brand TASCENSO ODT
Mechanism Sphingosine 1-phosphate receptor binding agent
Target Sphingosine 1-phosphate receptor
Route ORAL
Formulation TABLET, ORALLY DISINTEGRATING

Mechanism of action

Sphingosine 1-phosphate receptor binding agent

Primary target: Sphingosine 1-phosphate receptor

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. fingolimod hydrochloride Sphingosine 1-phosphate receptor agonist
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  4. ozanimod hydrochloride Sphingosine 1-phosphate receptor Edg-1 modulator
  5. siponimod Antineoplastic and immunomodulating agents (L04)
  6. etrasimod Antineoplastic and immunomodulating agents (L04)
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Frequently asked questions

What is fingolimod lauryl sulfate?

fingolimod lauryl sulfate (TASCENSO ODT) is a sphingosine 1-phosphate receptor binding agent. Associated with BICYCLE THERAPEUTICS. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for fingolimod lauryl sulfate?

TASCENSO ODT is a marketed brand name for fingolimod lauryl sulfate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of fingolimod lauryl sulfate?

fingolimod lauryl sulfate has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.