TheraRadar
Data updated: May 26, 2026

ZUSDURI (mitomycin)

Oncology Approved 2025-06-12

Zusduri is an alkylating medication used for adults with a specific form of bladder cancer that has returned. It helps patients with recurrent low-grade, intermediate-risk non-muscle invasive bladder cancer. This drug provides a therapeutic option for managing this particular stage and risk level of the disease.

Source: FDA Label • UROGEN PHARMA

How ZUSDURI Works

This medication works by preventing the synthesis of DNA within cells. It creates cross-links in the genetic material, a process that is influenced by the guanine and cytosine content of the target. When used at high concentrations, the drug also suppresses the production of cellular RNA and proteins.

1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-06-12
Patent Cliff
2031

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Routes
INTRAVESICAL
Dosage Forms
POWDER

Companies

Active Ingredient: MITOMYCIN

ZUSDURI Approval History

2026
Original
New Indication
New Form
Label Update
1 FDA actions from 2025 to 2025
Jun 2025 ORIGINAL
New Form · Type 3 - New Dosage Form

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

ZUSDURI Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

What's emerging in ZUSDURI's indications

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Phase 3 candidates targeting molecules with no FDA-approved drug, in indications ZUSDURI treats. First-in-class if their pivotal trials read out positive.

Drugs Similar to ZUSDURI

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

INLEXZO
GEMCITABINE HYDROCHLORIDE
1 shared
Johnson & Johnson
Shared indications:
Non-Muscle Invasive Bladder Cancer
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Clinical Trial Registry

25 trials
Trial Sponsor ID Phase Status Title
NCT06770582 NCI-2025-00008 NCI-2025-00008, NRG-GU014 Ph 2 recruiting Testing the Addition of the Immunotherapy Drug, Pembrolizumab, to Radiation Therapy Compared to the Usual Chemotherapy Treatment During Radiation Therapy for Bladder Cancer, PARRC Trial
NCT04929028 NCI-2021-06041 NCI-2021-06041, AMC-110 Ph 2 active not recruiting Therapy Adapted for High Risk and Low Risk HIV-Associated Anal Cancer
NCT04216290 NCI-2019-08628 NCI-2019-08628, EA8185 Ph 2 active not recruiting A Study of Chemotherapy and Radiation Therapy Compared to Chemotherapy and Radiation Therapy Plus MEDI4736 (Durvalumab) Immunotherapy for Bladder Cancer Which Has Spread to the Lymph Nodes, INSPIRE Trial
NCT07579195 RG1126354 NCI-2026-02920, FHIRB0021260 Ph 1, Ph 2 not yet recruiting Consolidative Therapy After EV + Pembrolizumab in Muscle Invasive Bladder Cancer, REINFORCE Trial
NCT04166318 EA2182 NCI-2019-02259, EA2182 Ph 2 active not recruiting Lower-Dose Chemoradiation in Treating Patients With Early-Stage Anal Cancer, the DECREASE Study
NCT07097142 NRG-GU015 NCI-2025-04136, NRG-GU015 Ph 3 recruiting Testing Shorter Duration Radiation Therapy Versus the Usual Radiation Therapy in Patients Receiving the Usual Chemotherapy Treatment for Bladder Cancer, ARCHER Study
NCT03775265 NCI-2018-03264 NCI-2018-03264, S1806 Ph 3 active not recruiting Chemoradiotherapy With or Without Atezolizumab in Treating Patients With Localized Muscle Invasive Bladder Cancer
NCT06704191 MC240502 UL1TR002377, NCI-2024-09555 Ph 1, Ph 2 recruiting In-home Intravesical Chemotherapy for the Treatment of Bladder Cancer, INVITE Trial
NCT05672108 22067 P30CA033572, NCI-2022-10436 Ph 2 recruiting Phase II Trial of Lung Chemoemobolization
NCT04329494 19184 NCI-2020-01254, 19184 Ph 1 recruiting PIPAC for the Treatment of Peritoneal Carcinomatosis in Patients With Ovarian, Uterine, Appendiceal, Colorectal, or Gastric Cancer
NCT07271355 24756 NCI-2025-08527, 24756 Ph 3 not yet recruiting Pressurized Intraperitoneal Aerosolized Chemotherapy With Mitomycin for the Treatment of Unresectable Appendix or Colorectal Cancer With Peritoneal Metastases, The IMPACT Trial
NCT04107077 IRB19-0160 Ph 2 recruiting Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer
NCT05024734 GAIN INST SZB-URO-21-001 Ph 2 recruiting Guiding Instillation in Non Muscle-invasive Bladder Cancer Based on Drug Screens in Patient Derived Organoids
NCT02891447 results posted 2016-0269 NCI-2018-02341, 2016-0269 Ph 2 completed Heated Mitomycin and Cisplatin During Surgery in Treating Patients With Stomach or Gastroesophageal Cancer
NCT00981656 results posted RTOG 0926 CDR0000654727, NCI-2011-01974 Ph 2 completed Radiation Therapy and Chemotherapy in Treating Patients With Stage I Bladder Cancer
NCT06462001 18UR004 Ph 3 active not recruiting BCG + MMC: Adding Mitomycin C to BCG in High-risk, Non-muscle-invasive Bladder Cancer
NCT06227065 POLO SZB-URO-24-001 Ph 2 not yet recruiting Precise Neoadjuvant Chemoresection of Low Grade NMIBC
NCT01004978 results posted NCI-2011-01981 NCI-2011-01981, ECOG-E1208 Ph 3 completed Chemoembolization With or Without Sorafenib Tosylate in Treating Patients With Liver Cancer That Cannot Be Removed by Surgery
NCT03617913 results posted MC1752 NCI-2018-01539, MC1752 Ph 2 completed Avelumab in Combination With Fluorouracil and Mitomycin or Cisplatin and Radiation Therapy in Treating Participants With Muscle-Invasive Bladder Cancer
NCT04845490 WUHIPEC02 UHCT-IEC-SOP-016-21-02 Ph 2 not yet recruiting Comparative Study of Mitomycin and Lobaplatin in Advanced Colorectal Cancer Patients With Radical Surgery Combined With Hyperthermic Intraperitoneal Chemotherapy
NCT01671488 276 results posted BrUOG 276 Ph 1, Ph 2 terminated A Phase I/II Evaluation of ADXS11-001, Mitomycin, 5-fluorouracil (5-FU) and IMRT for Anal Cancer
NCT01171482 07-2010-010 Ph 2 terminated Comparison Study of Sorafenib and 5-fluorouracil/Mitomycin for Metastatic Hepatocellular Carcinoma
NCT01017640 NCI-2012-01473 NCI-2012-01473, OSU-09100 Ph 1 completed Veliparib With or Without Mitomycin C in Treating Patients With Metastatic, Unresectable, or Recurrent Solid Tumors
NCT01843452 CHUV 20080214 Ph 2 terminated Phase II Study of Concomitant Intensity-modulated Radiotherapy Combined to Capecitabine, Mitomycin and Panitumumab in Patients With Stage II-IIIB Squamous-cell Carcinoma of the Anal Canal
NCT01953406 LUNG M_FM Ph 2 withdrawn The Efficacy of 5-fluorouracil/Mitomycin for the Patients With Pulmonary Metastasis of Hepatocellular Carcinoma
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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

Indications & Usage

FDA Label (PDF)

ZUSDURI is indicated for the treatment of Non-Muscle Invasive Bladder Cancer.

View full patent landscape →
4 OB patents · 2 families · 24 international docs across 6 countries

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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Revenue Insights

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Patent Timeline

  • Cliff: 2031
  • 4 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • 1 similar drugs
  • Same target/indication analysis
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Data Sources

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