yutrepia
yutrepia: developed by 1 company · 1 FDA decision.
yutrepia evidence translation
What we can confirm
1 FDA record
What it means
What to watch
Prepared research question
How could yutrepia → LQDA affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence1 indications · 0 study sponsors
Related indications
Study sponsors
No additional listed-company sponsor is linked.
Development Pipeline (1)
| Company | Phase |
|---|---|
| Liquidia Corp (LQDA) Pulmonary arterial hypertension (PAH) and pulmonary hyperten… | Approved |
FDA Decisions1 records
Frequently asked questions
Who is developing yutrepia?
yutrepia is being developed by Liquidia Corp.
What is yutrepia's latest FDA decision?
The most recent tracked FDA decision for yutrepia is Approval for 1 INDICATIONS AND USAGE • Pulmonary arterial hypertension (PAH; WHO Group 1) to improve exercise ability. Studies establishing effectiveness predominately included patients with NYHA Functional Class III symptoms and etiologies of idiopathic or heritable PAH (56%) or PAH associated with connective tissue diseases (33%). ( 1.1 ) • Pulmonary hypertension associated with interstitial lung disease (PH-ILD; WHO Group 3) to improve exercise ability. The study establishing effectiveness predominately i, dated May 23, 2025.