What is the plasma elimination half-life of empagliflozin (Jardiance)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 13, 2026 • View editorial policy

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.

Jardiance Half-Life

The plasma elimination half-life of empagliflozin (Jardiance) is approximately 12.4 hours based on population pharmacokinetic analysis. 1

Pharmacokinetic Details

The FDA label for Jardiance provides the most authoritative data on empagliflozin's elimination characteristics:

  • Terminal elimination half-life: 12.4 hours (apparent, based on population pharmacokinetic analysis) 1
  • Apparent oral clearance: 10.6 L/h at steady state 1
  • Time to steady state: Achieved after approximately 6 days of once-daily dosing, with up to 22% accumulation in plasma AUC 1

Supporting Research Data

Clinical studies have reported consistent half-life values:

  • In Chinese patients with type 2 diabetes, mean terminal elimination half-life values at steady state were 13.9 hours (10 mg dose) and 12.1 hours (25 mg dose) 2
  • Multiple-dose studies showed terminal half-life ranging from 10.3 to 18.8 hours 3
  • A Japanese study reported a terminal elimination half-life of 13.1 hours 4

Clinical Implications

The ~12-hour half-life supports:

  • Once-daily dosing: The half-life is sufficient to maintain therapeutic drug levels with once-daily administration 1
  • Urinary glucose excretion duration: Following single doses, the elevation in urinary glucose excretion approaches baseline by approximately 3 days for both 10 mg and 25 mg doses 1
  • Steady-state kinetics: Linear pharmacokinetics with no time-dependent characteristics, making dosing predictable 1

Important Caveat

The half-life remains relatively consistent across different patient populations, with no clinically meaningful alterations based on age, BMI, gender, race, or mild-to-moderate hepatic/renal impairment 1. However, drug exposure (AUC) does increase with declining renal function, though this doesn't substantially alter the elimination half-life itself.

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.