Exhibit 99.1

UroGen Pharma Reports First Quarter 2019 Financial Results and Recent
Corporate Developments
Recent Data Presentation Highlights Consistent Complete Response Rate and Strong Durability
atSix-Months in Evaluable Patients withLow-Grade Upper Tract Urothelial Cancer (LG UTUC)
Completion ofUGN-101 Rolling NDA Submission to the FDA On Track for 2H 2019
Pre-Commercial Activities and InfrastructureBuild-out Accelerate Ahead of Planned U.S.
Approval and Launch ofUGN-101 in 1H 2020
Conference Call and Webcast to be Held Today at 8:30 AM ET
NEW YORK, May 9, 2019 - UroGen Pharma Ltd. (Nasdaq:URGN), a clinical-stage biopharmaceutical company developing treatments to address unmet needs in uro-oncology, today announced financial results for the first quarter ended March 31, 2019 and provided an overview of the Company’s recent developments.
“The accomplishments and performance of UroGen during the first quarter have set the stage for a pivotal and exciting year ahead as we prepare for the potential approval and commercialization ofUGN-101, our first investigational candidate. Our top priority remains completion of our rolling New Drug Application (NDA) forUGN-101 for the treatment of patients withlow-grade upper tract urothelial cancer (LG UTUC) and, with our commercial preparations well underway, we are confident in our readiness to deliver on a strong launch in the first half of 2020,” said Liz Barrett, President and Chief Executive Officer of UroGen. “Our company sees great possibilities for the RTGel platform within uro-oncology, especially around new therapeutic modalities. Our goal is to leverage that and continue to build a company with sustainable growth via a robust pipeline as well as assessing opportunities via external partnerships.”
Recent Highlights
| • | | UGN-101 Clinical Development: |
| • | | At the 114th American Urological Association (AUA) Annual Meeting in Chicago, Seth Lerner, M.D. delivered a presentation during the plenary session that highlighted the unmet need and potential forUGN-101 to change the treatment paradigm for patients with LG UTUC. |
| • | | The updated analysis demonstrated that in the OLYMPUSintent-to-treat population, 71 patients had undergone primary disease evaluation (PDE) at the time of the analysis and 42 of the 71 patients (59 percent) achieved a complete response (CR).Forty-one patients enteredfollow-up. At the time of the analysis, 27 patients underwent asix-month evaluation, and 24 out of 27 patients (89 percent) have remained disease free at six months. The most common adverse events observed were urinary tract infection, ureteral narrowing and stricture formation. The majority of ureteral events were reported as mild to moderate and have resolved. Full Phase 3 data from the OLYMPUS trial is anticipated for 2H 2019. |