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Abrocitinib 100 mg (abrocitinib-100-mg)
Abrocitinib 100 mg (generic name: abrocitinib-100-mg) is a Janus kinase inhibitor drug developed by Pfizer. It is currently FDA-approved for Moderate to severe atopic dermatitis in adults who have had an inadequate response or intolerance to one or more biologics, or who are candidates for systemic therapy, Moderate to severe atopic dermatitis in children aged 12 years and older who have had an inadequate response or intolerance to one or more biologics, or who are candidates for systemic therapy.
Abrocitinib 100 mg, developed by Pfizer Inc., is a marketed drug for moderate to severe atopic dermatitis. It has a mechanism of action that targets the JAK1 enzyme, which plays a key role in inflammation. The drug has shown clinical differentiation in treating patients who have had an inadequate response or intolerance to one or more biologics. Its commercial significance is evident in its high revenue of $21.2B. Abrocitinib has undergone 6 trials and has been published in 45 publications. The drug's pipeline developments are not specified. Overall, Abrocitinib is a significant addition to the treatment options for atopic dermatitis.
At a glance
| Generic name | abrocitinib-100-mg |
|---|---|
| Sponsor | Pfizer |
| Drug class | Janus kinase inhibitor |
| Target | JAK1 |
| Therapeutic area | Immunology |
| Phase | FDA-approved |
| Annual revenue | 284 |
Approved indications
- Moderate to severe atopic dermatitis in adults who have had an inadequate response or intolerance to one or more biologics, or who are candidates for systemic therapy
- Moderate to severe atopic dermatitis in children aged 12 years and older who have had an inadequate response or intolerance to one or more biologics, or who are candidates for systemic therapy
Common side effects
- Nausea
- Gastrooesophageal reflux disease
- Pruritus
- Vomiting
- Pyrexia
- Alanine aminotransferase increased
- Cough
- Dermatitis atopic
- Gastritis
- Asthma
- Rosacea
- Hypotension
Drug interactions
- Warfarin
- Live vaccines
- Bacillus Calmette-Guérin (BCG) vaccine
- Other vaccines
- Vaccines
- Live or attenuated vaccines
- Vaccines (live)
- Vaccines (live or attenuated)
- Vaccines (live, attenuated, or inactivated)
- Vaccines (live, attenuated, or inactivated, or toxoid)
- Vaccines (live, attenuated, inactivated, or toxoid)
- Vaccines (live, attenuated, inactivated, toxoid, or subunit)
Key clinical trials
- Efficacy, Safety, and Tolerability of Abrocitinib in Subjects With Moderate to Severe Chronic Hand Eczema Refractory to Corticosteroid Therapy (PHASE2)
- Study to Evaluate Efficacy and Safety of PF-04965842 With or Without Topical Medications in Subjects Aged 12 Years and Older With Moderate to Severe Atopic Dermatitis (PHASE3)
- Study to Investigate the Efficacy of Abrocitinib in Adult Participants With Severe Fatigue From Post COVID Condition/Long COVID (PHASE2)
- Effects of Abrocitinib in Subjects With Atopic Dermatitis With an Unsatisfactory Response After Treatment With Dupilumab (PHASE4)
- Abrocitinib Expanded Access Protocol in Adolescents and Adults With Moderate to Severe Atopic Dermatitis
- A Study to Learn About Abrocitinib Tablets in People With Atopic Dermatitis in India (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
| SEC EDGAR | Revenue + earnings |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Abrocitinib 100 mg CI brief — competitive landscape report
- Abrocitinib 100 mg updates RSS · CI watch RSS
- Pfizer portfolio CI
Frequently asked questions about Abrocitinib 100 mg
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Related
- Drug class: All Janus kinase inhibitor drugs
- Target: All drugs targeting JAK1
- Manufacturer: Pfizer — full pipeline
- Therapeutic area: All drugs in Immunology
- Indication: Drugs for Moderate to severe atopic dermatitis in adults who have had an inadequate response or intolerance to one or more biologics, or who are candidates for systemic therapy
- Indication: Drugs for Moderate to severe atopic dermatitis in children aged 12 years and older who have had an inadequate response or intolerance to one or more biologics, or who are candidates for systemic therapy
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing