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Medical information resources

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This section contains selected medical information resources and does not constitute a complete summary of all available data. For additional information or to submit a specific request, please click the Contact us button below. This content is provided by UroGen Medical Affairs for US healthcare professionals only. Materials are scientific, non-promotional, and aligned with FDA-approved labeling. See full Prescribing Information below for complete product details.

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JELMYTO

ZUSDURI

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Administration / Preparation

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Device / Ancillary / Equipment

Safety / Disposal / Compatibility

Storage / Handling

ZUSDURI

Storage / Handling

Shelf Life of ZUSDURI Kit

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ZUSDURI

Safety / Disposal / Compatibility

Lab Abnormalities Reported in the ENVISION Clinical Trial

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ZUSDURI

Safety / Disposal / Compatibility

The Appropriate Disposal of ZUSDURI

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ZUSDURI

Safety / Disposal / Compatibility

Presence of Latex in ZUSDURI Packaging or Formulation

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ZUSDURI

Safety / Disposal / Compatibility

Effect of ZUSDURI on Sewer and Septic Systems

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ZUSDURI

Device / Ancillary / Equipment

Cleaning and Disinfecting of the Chilling Block (UCB0002)

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ZUSDURI

Clinical / Trials / Outcomes

Biopsy Procedure and Timing During the ENVISION Trial

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ZUSDURI

Clinical / Trials / Outcomes

Patients Excluded From Efficacy Analysis in ENVISION Trial

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ZUSDURI

Clinical / Trials / Outcomes

Patient-Reported Outcomes for ZUSDURI

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ZUSDURI

Clinical / Trials / Outcomes

Tumor Burden and Focality Efficacy in Phase 3 ENVISION Trial

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ZUSDURI

Clinical / Trials / Outcomes

Intent-to-Treat Population of Phase 3 ENVISION Trial

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ZUSDURI

Clinical / Trials / Outcomes

Phase 2b OPTIMA II Trial

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ZUSDURI

Clinical / Trials / Outcomes

Phase 3 ATLAS Trial

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ZUSDURI

Clinical / Trials / Outcomes

Phase 3 ENVISION Trial

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ZUSDURI

Administration / Preparation

Pharmacy Preparation of ZUSDURI

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ZUSDURI

Administration / Preparation

Additional Details Regarding the Administration of ZUSDURI

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ZUSDURI

Administration / Preparation

Sodium Bicarbonate as a Pre-Medication for ZUSDURI

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ZUSDURI

Administration / Preparation

Home Instillation of ZUSDURI

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JELMYTO

Storage / Handling

Shelf Life of the JELMYTO Kit

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JELMYTO

Storage / Handling

Extended in Use Storage Conditions and Handling of Reconstituted JELMYTO

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JELMYTO

Safety / Disposal / Compatibility

Presence of Latex in the JELMYTO Packaging or Formulation

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JELMYTO

Safety / Disposal / Compatibility

Appropriate Disposal for JELMYTO

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JELMYTO

Safety / Disposal / Compatibility

Effect of JELMYTO on Sewer and Septic Systems

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JELMYTO

Device / Ancillary / Equipment

Uroject12 Syringe Lever Used With the Instillation of JELMYTO

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JELMYTO

Device / Ancillary / Equipment

Updates Made to the Chilling Block Model

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JELMYTO

Device / Ancillary / Equipment

Cleaning, Disinfection, and Sterilization of the Uroject12 Syringe Lever

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JELMYTO

Device / Ancillary / Equipment

Cleaning of the New Model of the Chilling Block (UCB0002)

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JELMYTO

Clinical / Trials / Outcomes

Treatment of Ureteral Tumors Associated With Upper Tract Urothelial Carcinoma and JELMYTO

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JELMYTO

Clinical / Trials / Outcomes

OLYMPUS Long-Term Follow-Up Study (BL007)

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JELMYTO

Administration / Preparation

JELMYTO Administration Via Closed System Transfer Device

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JELMYTO

Administration / Preparation

Maintenance Treatment with JELMYTO

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For more information on what data we collect about you and how we use it, as well as information about the rights you may have under the California Consumer Privacy Act, please refer to our Privacy Policy.

This form is not intended for reporting adverse events or product complaints. To report suspected adverse events or product complaints, please call us at 1-855-987-6436. You are also encouraged to report side effects to the FDA. You can visit www.fda.gov/medwatch or call 1-800-FDA-1088.

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©2026 UroGen. All rights reserved. The information is intended for US healthcare professionals only. M-US-UGN-00068. Last updated June 2026.

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ZUSDURI™ (mitomycin) for intravesical solution Prescribing Information

JELMYTO® (mitomycin) for pyelocalyceal solution Prescribing Information

Report Adverse Reactions or Product Complaints

To report suspected adverse events or product complaints, please call us at 1‑855‑987‑6436.
You are also encouraged to report side effects to the FDA. You can visit www.fda.gov/medwatch or call 1‑800‑FDA‑1088.