NDAORALCAPSULE
Approved
Mar 2020
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
3
Data completeness
5/8 — Partial
Drug data last refreshed 8h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ZEPOSIA (ozanimod hydrochloride) is an oral sphingosine-1-phosphate (S1P) receptor modulator approved by the FDA in March 2020. It is indicated for patients with ulcerative colitis and Crohn's disease, conditions requiring immunomodulation to reduce inflammation in the gastrointestinal tract. The drug works by sequestering lymphocytes in lymphoid tissues, thereby reducing their infiltration into the inflamed bowel.
$63MPart D
Peak12.2 years to LOEZEPOSIA is in peak revenue phase with modest Part D spending ($63M in 2023), indicating a stable commercial footprint supporting a consolidated brand team focused on market penetration and patient retention.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (3)
Risk of Progressive Multifocal Leukoencephalopathy Among Patients With Multiple Sclerosis Exposed to Zeposia
Started Jun 2026
15 enrolled
Multiple SclerosisProgressive Multifocal Leukoencephalopathy
Ulcerative Colitis Leukocyte TRAfficking After Treatment With Zeposia: the ULTRAZ Study
Started Aug 2024
0Ulcerative Colitis
A Study Investigating the Utilization, Effectiveness and Quality of Life in Clinical Practice in Germany for Participants With Relapsing-remitting Multiple Sclerosis Treated With Ozanimod (Zeposia®)
Started Mar 2021
450 enrolled
Multiple Sclerosis, Relapsing-Remitting
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
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.