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Vibegron

Vibegron is a selective beta-3 adrenergic receptor agonist used primarily for the treatment of overactive bladder (OAB). It works by relaxing the detrusor muscle in the bladder, thereby reducing urinary urgency and frequency. While its direct impact on longevity is limited, managing OAB can significantly improve quality of life and reduce stress-related health issues.

Intelligence Profile

Research Papers

Vibegron, a medication used for overactive bladder (OAB), has been studied in various research papers and clinical trials.

A systematic review and network meta-analysis compared vibegron, mirabegron, and tolterodine, focusing on safety and efficacy for OAB patients. Though specific sample sizes aren't mentioned, meta-analyses generally pool data from multiple studies, offering robust insights. This review suggested that vibegron could be a comparably effective alternative with a favorable safety profile.

Another study reviewed treatments for refractory monosymptomatic enuresis in children, though vibegron's role specifically in enuresis remains less detailed, indicating a need for further exploration in pediatric cases.

A narrative review discussed managing persistent OAB symptoms in men with benign prostatic hyperplasia, mentioning vibegron as a therapeutic option. Despite limited specific data, this highlights the broad applicability of vibegron beyond typical OAB management.

In pediatric cases, a case report involving vibegron addressed anticholinergic-resistant neurogenic lower urinary tract dysfunction post-spinal cord amputation. This suggests potential uses in complex pediatric urological conditions.

Clinical trials further explore vibegron's potential. A phase 3 trial (NCT06987383) aims to study its effects on energy and resilience in aging, though not yet recruiting. An ongoing phase 2/3 study (NCT05491525) investigates its long-term safety in children with neurogenic detrusor overactivity on clean intermittent catheterization. A phase 4 trial (NCT05806164) compares vibegron with onabotulinumtoxinA for urgency urinary incontinence, actively recruiting participants to assess efficacy in real-world scenarios.

A terminated phase 1 trial (NCT01500382) explored the pharmacokinetics and pharmacodynamics of vibegron in women with OAB but did not reach completion. Meanwhile, a completed phase 3 study (NCT03583372) examined the long-term safety and tolerability in OAB patients.

Overall, vibegron shows promise across various demographics for managing OAB, though further targeted research would solidify these findings.

Disclaimer: This summary is for informational purposes only and should not be taken as medical advice. Always consult healthcare professionals for medical concerns.

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