Is Jubbonti safe for patients with impaired renal function undergoing dialysis?

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Last updated: November 27, 2025View editorial policy

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Jubbonti Safety in Dialysis Patients

I cannot provide a definitive recommendation regarding Jubbonti's safety in dialysis patients because no evidence was provided about Jubbonti specifically in the materials reviewed. The evidence presented discusses hepatitis C medications (glecaprevir/pibrentasvir, sofosbuvir-based regimens), SGLT2 inhibitors, and general medication management principles in dialysis patients, but does not mention Jubbonti.

Critical Information Gap

Without specific pharmacokinetic data, clinical trial evidence, or FDA labeling information for Jubbonti in patients with end-stage renal disease (ESRD) on dialysis, I cannot assess its safety profile in this population.

General Principles for Medication Safety in Dialysis Patients

While I cannot address Jubbonti specifically, the following framework should guide medication decisions in dialysis patients:

Key Considerations for Any Medication in Dialysis

  • Renal excretion pathway: Medications primarily eliminated renally require dose adjustment or may be contraindicated when eGFR <30 mL/min/1.73 m² 1

  • Dialyzability: Drugs removed during hemodialysis may require post-dialysis supplementation, though this is less relevant for peritoneal dialysis 2

  • Metabolite accumulation: Active or toxic metabolites that accumulate in renal failure pose significant safety concerns 1

  • Medication reconciliation: Dialysis patients are at heightened risk for adverse drug reactions due to polypharmacy and altered pharmacokinetics, making thorough medication review essential 1

What You Must Know About Jubbonti Before Use

To determine safety in dialysis patients, you need:

  1. Primary elimination route (renal vs. hepatic)
  2. Dialyzability characteristics (molecular weight, protein binding, volume of distribution)
  3. Metabolite profile and whether metabolites accumulate in renal failure
  4. FDA labeling for renal dosing recommendations
  5. Clinical trial data in patients with severe renal impairment (eGFR <30 mL/min/1.73 m²)

Practical Approach

Contact the manufacturer or consult the FDA-approved prescribing information for Jubbonti to obtain specific guidance on use in ESRD and dialysis patients. If no data exists, the medication should generally be avoided unless the benefit clearly outweighs unknown risks, and only after informed consent 1.

Close monitoring is mandatory if Jubbonti is used off-label in dialysis patients, with treatment rapidly interrupted if adverse effects occur 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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