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Data updated: Mar 10, 2026

ZEPOSIA

OZANIMOD HYDROCHLORIDE
Immunology Approved 2020-03-25

ZEPOSIA (ozanimod hydrochloride) is a sphingosine 1-phosphate receptor modulator indicated for use in adult patients. It is approved for the treatment of relapsing forms of multiple sclerosis, including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease. The medication is also used to treat adults with moderately to severely active ulcerative colitis.

Source: FDA Label • Bristol-Myers Squibb

How ZEPOSIA Works

Ozanimod binds with high affinity to sphingosine 1-phosphate (S1P) receptors 1 and 5. This action blocks the capacity of lymphocytes to egress from lymph nodes, which reduces the total number of lymphocytes circulating in the peripheral blood. The therapeutic effect in multiple sclerosis and ulcerative colitis may involve the reduction of lymphocyte migration into the central nervous system and the intestine.

Source: FDA Label
3
Indications
--
Phase 3 Trials
1
Priority Reviews
5
Years on Market

Details

Status
Prescription
First Approved
2020-03-25
Routes
ORAL
Dosage Forms
CAPSULE

Companies

Active Ingredient: OZANIMOD HYDROCHLORIDE

ZEPOSIA Approval History

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What ZEPOSIA Treats

2 indications

ZEPOSIA is approved for 2 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Relapsing forms of multiple sclerosis (clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease)
  • Moderately to severely active ulcerative colitis
Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

ZEPOSIA FDA Label Details

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Indications & Usage

FDA Label (PDF)

ZEPOSIA is indicated for the treatment of: • relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. • moderately to severely active ulcerative colitis (UC) in adults. ZEPOSIA is a sphingosine 1-phosphate receptor modulator indicated for the treatment of: • Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. • Moderately to severely active ulcerative colitis (UC) in adult...

ZEPOSIA Patents & Exclusivity

Latest Patent: Sep 2038
Exclusivity: Aug 2027

Patents (54 active)

US11680050 Expires Sep 30, 2038
US8481573 Expires Mar 24, 2033
US10239846 Expires Nov 15, 2030
US9382217 Expires May 14, 2029
US8796318 Expires May 14, 2029
+ 44 more patents

Exclusivity

M-309 Until Aug 2027
M-309 Until Aug 2027
M-309 Until Aug 2027
M-309 Until Aug 2027
M-309 Until Aug 2027
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.