What is the starting dose of Yorvipath?

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Last updated: December 12, 2025View editorial policy

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Starting Dose of Yorvipath

The recommended starting dose of Yorvipath (palopegteriparatide) is 18 μg/day administered subcutaneously, with subsequent titration based on serum calcium levels and clinical response. 1

Initial Dosing Protocol

  • Start at 18 μg/day subcutaneously as the standard initial dose for adult patients with hypoparathyroidism 1
  • Administer the dose once daily via subcutaneous injection 1
  • Titrate the dose alongside conventional therapy (calcitriol and calcium supplementation) based on individual patient response 1

Dose Titration Strategy

  • Adjust dosing based on serum calcium monitoring to maintain levels within the normal reference range (8.3-10.6 mg/dL) 1
  • The goal is to gradually reduce or eliminate conventional therapy requirements while maintaining normocalcemia 1
  • Dose adjustments should be individualized, with real-world data showing no clinically meaningful differences (>3 μg) in final doses between patients who switched directly from short-lived PTH therapy versus those who did not 1

Transitioning from Other PTH Therapies

  • Patients can transition directly from short-lived PTH or PTH-related protein therapy (such as teriparatide or recombinant human PTH [1-84]) to palopegteriparatide at the 18 μg/day starting dose 1
  • In real-world practice, approximately 50% of patients switched directly from short-lived PTH therapy without a washout period 1
  • Direct switching does not require dose modification from the standard 18 μg/day starting dose 1

Clinical Monitoring

  • Monitor serum calcium levels regularly during dose titration to ensure maintenance within normal range 1
  • Track conventional therapy requirements (calcitriol and calcium) as these should decrease over time with effective palopegteriparatide treatment 1
  • The proportion of patients achieving independence from conventional therapy (no calcitriol and ≤600 mg/day elemental calcium) increases progressively over 12 months of treatment 1

Safety Considerations

  • The 18 μg/day starting dose has demonstrated a favorable safety profile with no new safety signals identified in real-world use up to 12 months 1
  • Mean serum calcium levels remain within the normal reference range when starting at this dose 1

References

Research

Early U.S. Real-World Treatment Patterns and Outcomes in Palopegteriparatide Treatment for Patients With Hypoparathyroidism.

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists, 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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