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Baricitinib

Generic Name
Baricitinib
Brand Names
Olumiant
Drug Type
Small Molecule
Chemical Formula
C16H17N7O2S
CAS Number
1187594-09-7
Unique Ingredient Identifier
ISP4442I3Y

Overview

Baricitinib is a Janus kinase (JAK) inhibitor. JAKs are tyrosine protein kinases that play an important role in pro-inflammatory signaling pathways. Overactive JAKs have been implicated in autoimmune disorders, such as rheumatoid arthritis. By inhibiting the actions of JAK1 and JAK2, baricitinib attenuates JAK-mediated inflammation and immune responses. Baricitinib was first approved by the European Commission (EC) in February 2017 for the treatment of rheumatoid arthritis in adults and was later approved by the FDA in 2018. The EC later approved baricitinib for the treatment of atopic dermatitis, making it the first JAK inhibitor used for this indication in Europe. While baricitinib was granted emergency use as a treatment for COVID-19 in combination with remdesivir under the Emergency Use Authorization (EUA) in November 2020, the FDA fully approved the use of baricitinib for the treatment of COVID-19 in May 2022.

Indication

In the US and Europe, baricitinib is indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to one or more TNF blockers. Baricitinib may be used as monotherapy or in combination with methotrexate or other DMARDs. In Europe, baricitinib is indicated for the treatment of moderate to severe atopic dermatitis in adult patients who are candidates for systemic therapy. In the US, baricitinib is also indicated for the treatment of coronavirus disease 2019 (COVID-19) in hospitalized adults requiring supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation. Recently, it is also approved as the treatment for severe alopecia areata in adults.

Associated Conditions

  • Alopecia Areata (AA)
  • Coronavirus Disease 2019 (COVID‑19)
  • Severe Atopic Dermatitis
  • Moderate Atopic dermatitis
  • Moderate, active Rheumatoid arthritis
  • Severe, active Rheumatoid arthritis

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Eli Lilly and Company
0002-4479
ORAL
4 mg in 1 1
6/13/2022
Eli Lilly and Company
0002-6885
ORAL
4 mg in 1 1
12/20/2021
Eli Lilly and Company
0002-4732
ORAL
1 mg in 1 1
6/13/2022
Eli Lilly and Company
0002-4182
ORAL
2 mg in 1 1
6/13/2022

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
Authorised
2/13/2017

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
OLUMIANT FILM-COATED TABLET 4MG
SIN15505P
TABLET, FILM COATED
4.000mg
6/18/2018
OLUMIANT FILM-COATED TABLET 2MG
SIN15504P
TABLET, FILM COATED
2.000mg
6/18/2018

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
Baricitinib Tablets
国药准字HJ20215001
化学药品
片剂
4/29/2024
Baricitinib Tablets
国药准字HJ20190039
化学药品
片剂
4/29/2024
Baricitinib Tablets
国药准字H20234188
化学药品
片剂
9/28/2023

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
OLUMIANT baricitinib 4 mg film-coated tablet blister pack
277917
Medicine
A
1/23/2018
OLUMIANT baricitinib 2 mg film-coated tablet blister pack
277905
Medicine
A
1/23/2018

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