Business, energy, technology, markets and global industry news from Business News Today

urology

Medical Devices & Diagnostics

Is Avvio Medical building the next outpatient frontier in kidney stone and ureteral stone therapy?

Ureteral stones need faster care. Avvio Medical’s outpatient device tests whether microbubble lithotripsy can ease OR bottlenecks.

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Pharma & Biotech

Can vibegron strengthen Sumitomo Pharma America’s urology position after AUA 2026?

Older men with OAB and BPH remain hard to treat. Sumitomo Pharma America’s vibegron data may sharpen the next urology market test.

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Pharma & Biotech

NUBEQA data at AUA 2026 sharpens Bayer’s mCSPC positioning against androgen receptor rivals

Bayer has stronger NUBEQA mCSPC data. The tougher test is whether clinicians view ARASEC as confirmatory or merely supportive.

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Medical Devices & Diagnostics

Why BlueWind Medical’s $47.8m raise matters for the next phase of UUI treatment

UUI devices have clinical momentum. BlueWind Medical’s next challenge is proving Revi can scale through access, reimbursement, and workflow adoption.

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Medical Devices & Diagnostics

Did Aurie just crack the one-use catheter problem hospitals avoided for decades?

Single-use catheters finally face a regulated reuse challenge. Aurie’s FDA De Novo win could shift urology device economics.

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Medical Devices & Diagnostics

Why PanGIA Biotech’s urine biopsy data may matter more than the headline sensitivity figure suggests

PanGIA Biotech reported 97.8% sensitivity in a urine-based prostate cancer study. Read what the data changes and what risks still remain.

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Pharma & Biotech

ImmunityBio resubmits FDA application for ANKTIVA in bladder cancer after agency requests updated efficacy data

ImmunityBio has resubmitted its supplemental biologics license application to the U.S. Food and Drug Administration for ANKTIVA (nogapendekin alfa inbakicept) in combination with Bacillus Calmette-Guerin for BCG-unresponsive non-muscle invasive bladder cancer with papillary tumors, after the agency requested updated long-term efficacy data in March 2026. The resubmission follows a regulatory exchange that began in January

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