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uTRACT Jelmyto Registry: A Registry of Patients With Upper Tract Urothelial Cancer (UTUC) Treated With Jelmyto
RecruitingObservational study
uTRACT Jelmyto Registry: A Multicenter, Prospective and Retrospective Registry to Evaluate Real World Experience and Outcomes of Patients With Upper Tract Urothelial Cancer (UTUC) Treated With Jelmyto
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Adults \>18 years old and capable of giving informed consent. * Diagnosis of UTUC. * Receipt of at least 1 dose of JELMYTO after FDA approval (15 Apr 2020). Exclusion Criteria: * Incapable of giving informed consent (e.g., incarcerated individuals, individuals with dementia). * Receipt of 1 or more doses of JELMYTO (also referred to as UGN-101 or Mitogel in clinical development) before FDA approval (on or before 15 Apr 2020). * Pregnancy or lactation. * Unable to comply with protocol requirements (for prospective data capture). * Any medical or mental condition(s) that makes participation in the Registry inadvisable in the opinion of the Investigator (for prospective data capture).
About the study
The purpose of this registry is to evaluate real world experience and outcomes of patients with Upper Tract Urothelial Cancer (UTUC) treated with Jelmyto in the United States.
What is being tested
- Jelmyto (mitomycin) for pyelocalyceal solution (drug)
Sponsor: UroGen Pharma Ltd. · Participants: 450 · Started: Nov 17, 2023
Contact the study team
- Michael Louie, MD, MPH, MSc · Phone: 855-987-6436
Official record on ClinicalTrials.gov — NCT05874921
Locations in the U.S.
Conditions
- Urothelial (Transitional Cell) Carcinoma
- Neoplasms by Histologic Type
- Cancer (all types)
- Urologic Cancer
- Urogenital Cancer
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.