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AboutIntroducing Enbrel®Heritage of Enbrel®IndicationsTherapeutic IndicationsRheumatoid ArthritisJuvenile Idiopathic ArthritisPsoriatic ArthritisAxial SpondyloarthritisPsoriasis & Paediatric PsoriasisMechanism of actionMode of ActionHalf-lifeDosingDosingRheumatoid Arthritis, Psoriatic Arthritis & Axial SpondyloarthritisJuvenile Idiopathic ArthritisPsoriasisPaediatric PsoriasisAdministration & StorageAdministrationMYCLIC®StorageEfficacy & SafetyEfficacyRapid EffectivenessSustained EffectivenessEffectiveness With Monotherapy or Combination TherapySafetyTolerability Across IndicationsSummary of Prescribing InformationImmunogenicityImmunogenicity & Clinical ResponseImmunogenicity & Enbrel®Experience & InsightsExperience & InsightManufacturingPatient StoriesRheumatoid ArthritisPatient With an Increased Risk of Serious InfectionsMTX-IR PatientPatient Who Is Considering Starting a FamilyElderly-onset RA PatientYoung Patient Worried About the Lifelong Impact of RAYoung Patient Worried About Treatments That Lose Effectiveness Over TimeJuvenile Idiopathic ArthritisJuvenile PatientPatient Moving From Childhood to AdolescenceAxial SpondyloarthritisAS Patients With Heel EnthesitisAS Patients With Functional LimitationsAdvanced AS PatientsPsoriatic Arthritis & PsoriasisPsO Patient With Severe SymptomsPsO Patients With Cyclical SymptomsPsA Patient With Metabolic SyndromePsA Patient With Multiple Skin & Joint SymptomsSupport & ServicesSupport & ServicesUsing Enbrel®Summary of Prescribing InformationPatient ResourcesEventsMaterialsVideos

Psoriasis

Plaque PsO

    

Enbrel® was the first-approved biologic for both continuous and intermittent PsO therapies.1

    

The recommended dose of Enbrel® for adult patients with plaque PsO is2:

  • 25 mg BIW or
     
  • 50 mg QW or
     
  • 50 mg BIW for up to 12 weeks followed, if necessary, by2:
     
    • 25 mg BIW, or
       
    • 50 mg QW

    

Treatment with Enbrel® should continue for up to 24 weeks until remission is achieved. Continuous therapy beyond 24 weeks may be appropriate for some adult patients with PsO. Treatment should be discontinued in patients with PsO who show no response after 12 weeks. If re-treatment with Enbrel® is indicated, the same guidance on treatment duration should be followed. The dose should be 25 mg BIW or 50 mg QW.2

    

    

BIW, twice a week; PsO, psoriasis; QW, once a week; TNFR, tumour necrosis factor receptor.

    

References:Enbrel license extended to continuous treatment of psoriasis. News release. July 28, 2009. PharmaTimes online. Accessed May 5, 2022. http://www.pharmatimes.com/news/enbrel_license_extended_to_continuous_treatment_of_psoriasis_983939Enbrel. Local product document. Version LPDENB062021.

    

Please click the Prescribing Information link to view the safety and adverse events information of Enbrel®.
For the use only of Registered Medical Practitioners or a Hospital or a Laboratory.

    

PP-ENB-IND-0814 August 2022

    

Dosing
Badge Enbrel® mechanism of Action

Enbrel® is a soluble tumour necrosis factor receptor fusion protein

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Address: The Capital, A Wing, 1802, 18th Floor, Plot No. C-70, 'G' Block, Bandra Kurla Complex, Bandra East, Mumbai - 400051.


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