Palopegteriparatide Treatment Improves Renal Function in Adults with Chronic Hypoparathyroidism: 1-Year Results from the Phase 3 PaTHway Trial

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Lars Rejnmark - , Aarhus University (Author)
  • Elvira O. Gosmanova - , Albany Medical College (Author)
  • Aliya A. Khan - , McMaster University (Author)
  • Noriko Makita - , The University of Tokyo (Author)
  • Yasuo Imanishi - , Osaka Metropolitan University (Author)
  • Yasuhiro Takeuchi - , Toranomon Hospital (Author)
  • Stuart Sprague - , The University of Chicago (Author)
  • Dolores M. Shoback - , University of California at San Francisco (Author)
  • Lynn Kohlmeier - , Providence (Author)
  • Mishaela R. Rubin - , Columbia University (Author)
  • Andrea Palermo - , Universita Campus Bio-Medico di Roma (Author)
  • Peter Schwarz - , Righospitalet (Author)
  • Claudia Gagnon - , Université Laval (Author)
  • Elena Tsourdi - , Department of Internal Medicine III (Author)
  • Carol Zhao - , Ascendis Pharma (Author)
  • Michael A. Makara - , Ascendis Pharma (Author)
  • Michael S. Ominsky - , Ascendis Pharma (Author)
  • Bryant Lai - , Ascendis Pharma (Author)
  • Jenny Ukena - , Ascendis Pharma (Author)
  • Christopher T. Sibley - , Ascendis Pharma (Author)
  • Aimee D. Shu - , Ascendis Pharma (Author)

Abstract

Introduction: Individuals with chronic hypoparathyroidism managed with conventional therapy (active vitamin D and calcium) have an increased risk for renal dysfunction versus age- and sex-matched controls. Treatments that replace the physiologic effects of parathyroid hormone (PTH) while reducing the need for conventional therapy may help prevent a decline in renal function in this population. This post hoc analysis examined the impact of palopegteriparatide treatment on renal function in adults with chronic hypoparathyroidism. Methods: PaTHway is a phase 3 trial of palopegteriparatide in adults with chronic hypoparathyroidism that included a randomized, double-blind, placebo-controlled 26-week period followed by an ongoing 156-week open-label extension (OLE) period. Changes in renal function over 52 weeks (26 weeks blinded + 26 weeks OLE) were assessed using estimated glomerular filtration rate (eGFR). A subgroup analysis was performed with participants stratified by baseline eGFR < 60 or ≥ 60 mL/min/1.73 m2. Results: At week 52, over 95% (78/82) of participants remained enrolled in the OLE and of those, 86% maintained normocalcemia and 95% achieved independence from conventional therapy (no active vitamin D and ≤ 600 mg/day of calcium), with none requiring active vitamin D. Treatment with palopegteriparatide over 52 weeks resulted in a mean (SD) increase in eGFR of 9.3 (11.7) mL/min/1.73 m2 from baseline (P < 0.0001) and 43% of participants had an increase ≥ 10 mL/min/1.73 m2. In participants with baseline eGFR < 60 mL/min/1.73 m2, 52 weeks of treatment with palopegteriparatide resulted in a mean (SD) increase of 11.5 (11.3) mL/min/1.73 m2 (P < 0.001). One case of nephrolithiasis was reported for a participant in the placebo group during blinded treatment; none were reported through week 52 with palopegteriparatide. Conclusion: In this post hoc analysis of the PaTHway trial, palopegteriparatide treatment was associated with significantly improved eGFR at week 52 in addition to previously reported maintenance and normalization of serum and urine biochemistries. Further investigation of palopegteriparatide for the preservation of renal function in hypoparathyroidism is warranted. Trial Registration: ClinicalTrials.gov NCT04701203.

Details

Original languageEnglish
Pages (from-to)2500-2518
Number of pages19
JournalAdvances in therapy
Volume41
Issue number6
Early online date30 Apr 2024
Publication statusPublished - Jun 2024
Peer-reviewedYes

External IDs

PubMed 38691316

Keywords

ASJC Scopus subject areas

Keywords

  • Clinical trial, Glomerular filtration rate, Hypoparathyroidism, Kidney, Palopegteriparatide, Parathyroid hormone, Renal disease, TransCon PTH