Tenapanor as Therapy for Hyperphosphatemia in Maintenance Dialysis Patients: Results from the OPTIMIZE Study

Kidney360. 2024 May 1;5(5):732-742. doi: 10.34067/KID.0000000000000387. Epub 2024 Feb 7.

Abstract

Key Points:

  1. Tenapanor, a first-in-class local inhibitor of sodium/hydrogen exchanger isoform 3, acts as a phosphate absorption inhibitor by decreasing paracellular phosphate absorption.

  2. Tenapanor alone or with phosphate binders achieved P ≤ 5.5 mg/dl over 10 weeks in 34%–38% of patients taking phosphate binders at baseline.

  3. Tenapanor can help adults with CKD on maintenance dialysis achieve normal serum phosphate concentrations.

Background: OPTIMIZE was a randomized, open-label study evaluating different tenapanor initiation methods. OPTIMIZE evaluated tenapanor alone and in combination with phosphate binders (PBs) to achieve target serum phosphate (P) ≤5.5 mg/dl.

Methods: Patients with inadequately controlled P receiving maintenance dialysis from 42 US locations who were taking PBs with baseline P > 5.5 mg/dl and ≤ 10.0 mg/dl, or were PB-naive with baseline P > 4.5 mg/dl and ≤ 10.0 mg/dl, were included in OPTIMIZE. Participants taking PBs at baseline were randomized to switch from PBs to tenapanor (Straight Switch; n=151) or reduce PB dosage by ≥50% and add tenapanor (Binder Reduction; n=152); PB-naive patients started tenapanor alone (Binder-Naive; n=30). Participants received tenapanor 30 mg twice a day for 10 weeks (part A), followed by an elective, 16-week open-label extension (part B). Outcomes included changes from baseline in P, intact fibroblast growth factor 23, parathyroid hormone, serum calcium, and medication burden; patient-reported outcomes; and safety.

Results: By part A end point, 34.4% (Straight Switch), 38.2% (Binder Reduction), and 63.3% (Binder-Naive) of patients achieved P ≤ 5.5 mg/dl. Mean P reduction and median pill burden reduction from baseline to part A end point were 0.91±1.7 mg/dl and 4 pills/d for the Straight Switch and 0.99±1.8 mg/dl and 1 pill/d for the Binder Reduction group. The mean P reduction for Binder-Naive patients was 0.87±1.5 mg/dl. Among Straight Switch and Binder Reduction patients who completed patient experience questionnaires, 205 of 243 (84.4%) reported an improved phosphate management routine. Diarrhea was the most common adverse event (133 of 333 [39.9%]).

Conclusions: Tenapanor as monotherapy or in combination with PBs effectively lowered P toward the target range in patients who were PB-naive or who were not at goal despite PB use.

Clinical Trial registration number: NCT04549597.

Trial registration: ClinicalTrials.gov NCT02081534 NCT02675998 NCT03427125 NCT03824587 NCT03988920 NCT04549597.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Female
  • Humans
  • Hyperphosphatemia* / etiology
  • Hyperphosphatemia* / therapy
  • Isoquinolines / therapeutic use
  • Male
  • Middle Aged
  • Renal Dialysis* / adverse effects
  • Sulfonamides / therapeutic use
  • Treatment Outcome

Substances

  • Isoquinolines
  • Sulfonamides

Associated data

  • ClinicalTrials.gov/NCT02081534
  • ClinicalTrials.gov/NCT02675998
  • ClinicalTrials.gov/NCT03427125
  • ClinicalTrials.gov/NCT03824587
  • ClinicalTrials.gov/NCT03988920
  • ClinicalTrials.gov/NCT04549597

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