EOHILIA (budesonide) by Takeda is corticosteroid hormone receptor agonists [moa]. Approved for corticosteroid [epc]. First approved in 2024.
Drug data last refreshed 3h ago · AI intelligence enriched 1mo ago
EOHILIA is an oral budesonide suspension approved by the FDA on February 9, 2024, as a corticosteroid hormone receptor agonist. It treats inflammatory conditions through local corticosteroid action in the gastrointestinal tract. The mechanism involves binding to corticosteroid receptors to reduce inflammation and immune response.
Early-stage commercial trajectory with moderate competitive pressure (30%) suggests active team building for sales, marketing, and medical affairs expansion.
Corticosteroid Hormone Receptor Agonists
Corticosteroid
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Dose Ranging Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Budesonide Rectal Foam in Pediatric Patients Aged 5 to 17 Years With Active, Mild to Moderate Distal Ulcerative Colitis
QUARTZ: Comparative Effectiveness of Switching From Albuterol to Albuterol/Budesonide Versus Adding Low-dose ICS or LTRA to Albuterol
A Study to Investigate How Budesonide and Formoterol Move Through the Body (Pharmacokinetics) When Delivered With Different Devices in Participants Aged 4 to Less Than 12 Years Old With Asthma
A Study to Investigate the Effect of Budesonide/Glycopyrronium/Formoterol Fumarate Metered Dose Inhaler (BGF MDI) Compared With Placebo MDI on Heart and Lung Function in Participants With Chronic Obstructive Pulmonary Disease (COPD) and Hyperinflation
Pooled Analysis of Single-arm Studies of Budesonide/Glycopyrronium/Formoterol (BGF) in Routine Care Setting
Worked on EOHILIA at Takeda? Share your interview experience or compensation data (+7 days Pro)
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
Upgrade to Pro to access patent cliff timelines and LOE dates and other premium pharma intelligence.
Upgrade to Pro — $25/moUpgrade to Pro to access CMS Part B ASP pricing data and other premium pharma intelligence.
Upgrade to Pro — $25/moEOHILIA represents a growth-stage launch opportunity within Takeda's corticosteroid portfolio, offering roles in commercial execution, market access, and medical education. The 12.3-year patent exclusivity provides career stability for brand team members willing to commit to long-term product development.