baricitinib
baricitinib: developed by 1 company · 33 clinical trials tracked · 1 FDA decision.
baricitinib evidence translation
What we can confirm
1 FDA record · 33 tracked trials
What it means
What to watch
Prepared research question
How could baricitinib → LLY affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence8 indications · 1 study sponsors
Related indications
Study sponsors
Development Pipeline (2)
| Company | Phase |
|---|---|
| ELI LILLY & Co (LLY) In collaboration with Incyte Corporation, for the treatment … | Approved |
| ELI LILLY & Co (LLY) for the treatment of adults with moderately to severely acti… | Approved |
Clinical Trials (33)showing 10 most recent
A Randomised Platform Trial to Evaluate Therapeutics in Patients With Moderate or Severe Dengue (DEN-HOST)
Primary endpoint: Progression to severe dengue/critical dengue
Baricitinib Curative Repression of HIV-1
Primary endpoint: Time to restart ART
A Phase IIa, Single-Site, Open-Label Trial of Baricitinib in Patients With Cardiac Sarcoidosis
Primary endpoint: Proportion of patients with resolution of cardiac FDG uptake on PET-CT
A Phase 3, Double-Blind, Randomized, Placebo-Controlled Study of Baricitinib to Preserve Beta Cell Function in Participants Newly Diagnosed With Type 1 Diabetes Aged ≥1 to <36 Years
Primary endpoint: Change from Baseline in C-peptide Area Under the Curve (AUC)
A Phase 3, Double-Blind, Randomized, Placebo-Controlled Study of Baricitinib to Delay Stage 3 Type 1 Diabetes in At-risk Participants Aged ≥1 to <36 Years
Primary endpoint: Time from Baseline to Diagnosis of Stage 3 Type 1 Diabetes
Justification And Evaluation of Baricitinib Plus Corticosteroids Versus corticosteroiDs Alone in pOlymyalgia RhEumatica - JADORE-BARI Study
Primary endpoint: Following of the Polymyalgia Rheumatica Activity score
Randomized Double-Blind Placebo-Controlled Trial EValuating Baricitinib on PERSistent NEurologic and Cardiopulmonary Symptoms of Long COVID (REVERSE-LC)
Primary endpoint: CNS-Vital Signs Global Cognitive Index
A Pilot Study to Evaluate the Safety and Efficacy of Baricitinib in the Treatment of Frontal Fibrosing Alopecia (FFA)
Primary endpoint: 30% Change in Lichen Planopilaris Activity (LPPAI) Scores
Janus Kinase-STAT Inhibition to Reduce APOL1 Associated Kidney Disease
Primary endpoint: Percent change in albuminuria (UACR)
A Phase 3, Double-Blind, Randomized, Placebo-Controlled Trial to Evaluate the Efficacy, Safety, and Pharmacokinetics (PK) of Baricitinib in Children From 6 Years to Less Than 18 Years of Age With Alopecia Areata
Primary endpoint: Percentage of Participants Achieving an Absolute Severity of Alopecia Tool (SALT) ≤20
Frequently asked questions
Who is developing baricitinib?
baricitinib is being developed by ELI LILLY & Co.
How many clinical trials involve baricitinib?
BioSniper tracks 33 clinical trials involving baricitinib.
What is baricitinib's latest FDA decision?
The most recent tracked FDA decision for baricitinib is Approval, dated May 31, 2018.