Reports Q2 revenue $24.215M, consensus $23.13M. “The recent FDA approval of ZUSDURI for the treatment of adults with recurrent LG-IR-NMIBC represents a truly transformative milestone for patients and for UroGen, marking our evolution into a multi-product uro-oncology company and our leadership in the field,” said Liz Barrett, President and Chief Executive Officer of UroGen. “Our commercial team is enthusiastically executing the ZUSDURI launch plan as we scale the organization to address the estimated $5 billion+ market opportunity. JELMYTO for pyelocalyceal solution, our treatment for low-grade upper tract urothelial carcinoma, continues to grow with strong underlying demand in the second quarter reflecting continued interest in this important therapy for patients. We are equally excited about the continued progress across our pipeline, including our next-generation mitomycin formulations and immuno-oncology candidates. With a solid balance sheet, we are well positioned to fully support the launch of ZUSDURI while advancing strategic business initiatives to drive sustained growth and innovation.”
Elevate Your Investing Strategy:
- Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on URGN:
- UroGen Pharma announces 24-month DOR for Phase 3 ENVISION trial
- UroGen Pharma announces publication of Phase 3b ZUSDURI study results
- UroGen Pharma announces five-year long-term extension study of ZUSDURI
- UroGen Pharma call volume above normal and directionally bullish
- UroGen Pharma’s Promising Outlook: Buy Rating Backed by Clinical Success and FDA Approvals