TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ZUSDURI

MITOMYCIN
Oncology Approved 2025-06-12
1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-06-12
Routes
INTRAVESICAL
Dosage Forms
POWDER

Companies

Active Ingredient: MITOMYCIN

ZUSDURI Approval History

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What ZUSDURI Treats

1 indications

ZUSDURI is approved for 1 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Non-Muscle Invasive Bladder Cancer
Source: FDA Label

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Active Pipeline

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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.

ZUSDURI FDA Label Details

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Indications & Usage

FDA Label (PDF)

ZUSDURI™ is indicated for the treatment of adult patients with recurrent low-grade intermediate-risk non-muscle invasive bladder cancer (LG-IR-NMIBC). ZUSDURI is an alkylating drug indicated for the treatment of adult patients with recurrent low-grade intermediate-risk non-muscle invasive bladder cancer (LG-IR-NMIBC).

ZUSDURI Patents & Exclusivity

Latest Patent: Jan 2031
Exclusivity: Jun 2028

Patents (4 active)

US10039832 Expires Jan 20, 2031
US9950069 Expires Jan 20, 2031
US9040074 Expires Jan 20, 2031
US12440568 Expires Jan 20, 2031

Exclusivity

NP Until Jun 2028
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.