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Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study

The standard treatment of primary hypoparathyroidism (hypoPT) with oral calcium supplementation and calcitriol (or an analog), intended to control hypocalcemia and hyperphosphatemia and avoid hypercalciuria, remains challenging for both patients and clinicians. In 2015, human parathyroid hormone (hP...

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Autores principales: Ish‐Shalom, Sofia, Caraco, Yoseph, Khazen, Nariman Saba, Gershinsky, Michal, Szalat, Auryan, Schwartz, Phillip, Arbit, Ehud, Galitzer, Hillel, Tang, Jonathan CY, Burshtein, Gregory, Rothner, Ariel, Raskin, Arthur, Blum, Miriam, Fraser, William D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252608/
https://www.ncbi.nlm.nih.gov/pubmed/33666947
http://dx.doi.org/10.1002/jbmr.4274
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author Ish‐Shalom, Sofia
Caraco, Yoseph
Khazen, Nariman Saba
Gershinsky, Michal
Szalat, Auryan
Schwartz, Phillip
Arbit, Ehud
Galitzer, Hillel
Tang, Jonathan CY
Burshtein, Gregory
Rothner, Ariel
Raskin, Arthur
Blum, Miriam
Fraser, William D
author_facet Ish‐Shalom, Sofia
Caraco, Yoseph
Khazen, Nariman Saba
Gershinsky, Michal
Szalat, Auryan
Schwartz, Phillip
Arbit, Ehud
Galitzer, Hillel
Tang, Jonathan CY
Burshtein, Gregory
Rothner, Ariel
Raskin, Arthur
Blum, Miriam
Fraser, William D
author_sort Ish‐Shalom, Sofia
collection PubMed
description The standard treatment of primary hypoparathyroidism (hypoPT) with oral calcium supplementation and calcitriol (or an analog), intended to control hypocalcemia and hyperphosphatemia and avoid hypercalciuria, remains challenging for both patients and clinicians. In 2015, human parathyroid hormone (hPTH) (1‐84) administered as a daily subcutaneous injection was approved as an adjunctive treatment in patients who cannot be well controlled on the standard treatments alone. This open‐label study aimed to assess the safety and efficacy of an oral hPTH(1‐34) formulation as an adjunct to standard treatment in adult subjects with hypoparathyroidism. Oral hPTH(1‐34) tablets (0.75 mg human hPTH(1‐34) acetate) were administered four times daily for 16 consecutive weeks, and changes in calcium supplementation and alfacalcidol use, albumin‐adjusted serum calcium (ACa), serum phosphate, urinary calcium excretion, and quality of life throughout the study were monitored. Of the 19 enrolled subjects, 15 completed the trial per protocol. A median 42% reduction from baseline in exogenous calcium dose was recorded (p = .001), whereas median serum ACa levels remained above the lower target ACa levels for hypoPT patients (>7.5 mg/dL) throughout the study. Median serum phosphate levels rapidly decreased (23%, p = .0003) 2 hours after the first dose and were maintained within the normal range for the duration of the study. A notable, but not statistically significant, median decrease (21%, p = .07) in 24‐hour urine calcium excretion was observed between the first and last treatment days. Only four possible drug‐related, non‐serious adverse events were reported over the 16‐week study, all by the same patient. A small but statistically significant increase from baseline quality of life (5%, p = .03) was reported by the end of the treatment period. Oral hPTH(1‐34) treatment was generally safe and well tolerated and allowed for a reduction in exogenous calcium supplementation, while maintaining normocalcemia in adult patients with hypoparathyroidism. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
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spelling pubmed-82526082021-07-09 Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study Ish‐Shalom, Sofia Caraco, Yoseph Khazen, Nariman Saba Gershinsky, Michal Szalat, Auryan Schwartz, Phillip Arbit, Ehud Galitzer, Hillel Tang, Jonathan CY Burshtein, Gregory Rothner, Ariel Raskin, Arthur Blum, Miriam Fraser, William D J Bone Miner Res Original Articles The standard treatment of primary hypoparathyroidism (hypoPT) with oral calcium supplementation and calcitriol (or an analog), intended to control hypocalcemia and hyperphosphatemia and avoid hypercalciuria, remains challenging for both patients and clinicians. In 2015, human parathyroid hormone (hPTH) (1‐84) administered as a daily subcutaneous injection was approved as an adjunctive treatment in patients who cannot be well controlled on the standard treatments alone. This open‐label study aimed to assess the safety and efficacy of an oral hPTH(1‐34) formulation as an adjunct to standard treatment in adult subjects with hypoparathyroidism. Oral hPTH(1‐34) tablets (0.75 mg human hPTH(1‐34) acetate) were administered four times daily for 16 consecutive weeks, and changes in calcium supplementation and alfacalcidol use, albumin‐adjusted serum calcium (ACa), serum phosphate, urinary calcium excretion, and quality of life throughout the study were monitored. Of the 19 enrolled subjects, 15 completed the trial per protocol. A median 42% reduction from baseline in exogenous calcium dose was recorded (p = .001), whereas median serum ACa levels remained above the lower target ACa levels for hypoPT patients (>7.5 mg/dL) throughout the study. Median serum phosphate levels rapidly decreased (23%, p = .0003) 2 hours after the first dose and were maintained within the normal range for the duration of the study. A notable, but not statistically significant, median decrease (21%, p = .07) in 24‐hour urine calcium excretion was observed between the first and last treatment days. Only four possible drug‐related, non‐serious adverse events were reported over the 16‐week study, all by the same patient. A small but statistically significant increase from baseline quality of life (5%, p = .03) was reported by the end of the treatment period. Oral hPTH(1‐34) treatment was generally safe and well tolerated and allowed for a reduction in exogenous calcium supplementation, while maintaining normocalcemia in adult patients with hypoparathyroidism. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). John Wiley & Sons, Inc. 2021-03-05 2021-06 /pmc/articles/PMC8252608/ /pubmed/33666947 http://dx.doi.org/10.1002/jbmr.4274 Text en © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Ish‐Shalom, Sofia
Caraco, Yoseph
Khazen, Nariman Saba
Gershinsky, Michal
Szalat, Auryan
Schwartz, Phillip
Arbit, Ehud
Galitzer, Hillel
Tang, Jonathan CY
Burshtein, Gregory
Rothner, Ariel
Raskin, Arthur
Blum, Miriam
Fraser, William D
Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study
title Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study
title_full Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study
title_fullStr Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study
title_full_unstemmed Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study
title_short Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study
title_sort safety and efficacy of oral human parathyroid hormone (1‐34) in hypoparathyroidism: an open‐label study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252608/
https://www.ncbi.nlm.nih.gov/pubmed/33666947
http://dx.doi.org/10.1002/jbmr.4274
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