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AboutAboutHow Cibinqo worksIntroducing CibinqoMOA OverviewAtopic DermatitisPatient ProfilesPatient Profiles OverviewPatient Profile 1Patient Profile 2Patient Profile 3Patient Profile 4EfficacyEfficacyClinical EfficacyStudy OverviewJADE COMPAREJADE MONOJADE REGIMENJADE TEENJADE EXTENDJADE DARESafety
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Information on how to access Cibinqo®▼ (abrocitinib) prescribing information and adverse event reporting can be found at the bottom of the page. 
Updated Safety Recommendation - Abrocitinib should only be used if no suitable treatment alternatives are available in patients: 65 years of age and older, patients with history of atherosclerotic cardiovascular disease or other cardiovascular risk factors (such as current or past long-time smokers), patients with malignancy risk factors (e.g. current malignancy or history of malignancy). (Cibinqo Summary of Product Characteristics)

Cibinqo – a once daily, oral option to treat your patients' moderate-to-severe atopic dermatitis (AD)

For patients aged 12 years and older with moderate-to-severe AD who are candidates for systemic therapy1

Atopic dermatitis mechanism of disease​​​​​​​Explore more​​​​​​​MOA overview

Learn more
about JAK inhibition, the role of the JAK/STAT pathway and how Cibinqo works.
 

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Patient profiles

Discover which patients may be suitable for treatment with Cibinqo.


 

Learn moreLoadingAtopic dermatitis 

Read more on the Atopic Dermatitis disease area on our above brand therapy area page.

 

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AD=atopic dermatitis; MOA= Mode of action; JAK= Janus kinase; STAT= Signal transducer and activator of transcription.Prescribing information:
Cibinqo (abrocitinib) Prescribing Information (Great Britain)

References:

Cibinqo (abrocitinib) Summary of Product Characteristics.
PP-CIB-GBR-0804. April 2023.

Cibinqo Risk Minimisation Programme (RMP) materials, including a Patient Card and Prescriber Brochure, are available from https://www.medicines.org.uk/emc/product/12874/rmms. Patients treated with Cibinqo should be given the Patient Card.

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

for MHRA Yellow Card in Google Play or Apple App Store

 

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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