Wednesday, July 8, 2026

Drug profile · INN

abrocitinib

abrocitinib (CIBINQO) is a tyrosine-protein kinase jak1 inhibitor. Route of administration: oral. Current US regulatory status: approved.

FDA: approved EMA: approved PMDA: approved Dermatologicals (D11) D11AH08
US status approved
Patents linked 0
Pipeline programs 3
News articles 0
Drug details — abrocitinib
US status
approved
Class
Dermatologicals (D11)
Route
ORAL
Patents
0
Programs
3
Data quality
0.84

Quick answer

abrocitinib (CIBINQO) is a tyrosine-protein kinase jak1 inhibitor. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN abrocitinib
Brand CIBINQO
Mechanism Tyrosine-protein kinase JAK1 inhibitor
Target Tyrosine-protein kinase JAK1
Therapeutic class Dermatologicals (D11)
Route ORAL
Formulation TABLET
ATC code D11AH08

Mechanism of action

Tyrosine-protein kinase JAK1 inhibitor

Primary target: Tyrosine-protein kinase JAK1

Approval history

Authority Status Date
FDA approved
EMA approved
PMDA approved

Pipeline programs

  1. Abrocitinib Phase 3 · First Biotech (Australia) · Moderate-to-Severe Atopic Dermatitis
  2. Abrocitinib Placebo, Abrocitinib Phase 3 · First Biotech (Australia) · Moderate-to-Severe Atopic Dermatitis
  3. B7451015 Phase 3 · First Biotech (Australia) · Moderate to severe atopic dermatitis

Related & competitor drugs

  1. beremagene geperpavec Dermatologicals (D03)
  2. dupilumab Dermatologicals (D11)
  3. imiquimod Dermatologicals (D06)
  4. lebrikizumab Dermatologicals (D11)
  5. retapamulin Dermatologicals (D06)
  6. tacrolimus Dermatologicals (D11)

Frequently asked questions

What is abrocitinib?

abrocitinib (CIBINQO) is a tyrosine-protein kinase jak1 inhibitor. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for abrocitinib?

CIBINQO is a marketed brand name for abrocitinib. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of abrocitinib?

abrocitinib 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.