Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study
ABSTRACT 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 ho...
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creator | 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 |
description | ABSTRACT
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). |
doi_str_mv | 10.1002/jbmr.4274 |
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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).</description><identifier>ISSN: 0884-0431</identifier><identifier>EISSN: 1523-4681</identifier><identifier>DOI: 10.1002/jbmr.4274</identifier><identifier>PMID: 33666947</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>25-Hydroxyvitamin D ; Acetic acid ; Adult ; Adverse events ; Calcitriol ; Calcium ; Calcium (blood) ; Calcium (urinary) ; Calcium phosphates ; CALCIUM/PHOSPHATE DISORDERS ; Dietary supplements ; Dosage ; Excretion ; Humans ; Hypercalciuria ; Hyperphosphatemia ; Hypocalcemia ; HYPOPARATHYROIDISM ; Hypoparathyroidism - drug therapy ; Normocalcemia ; ORAL PARATHYROID HORMONE ; Original ; Parathyroid ; PARATHYROID HORMONE ; Parathyroid Hormone - adverse effects ; PARATHYROID‐RELATED DISORDERS ; Quality of Life ; Statistical analysis ; Teriparatide - adverse effects</subject><ispartof>Journal of bone and mineral research, 2021-06, Vol.36 (6), p.1060-1068</ispartof><rights>2021 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR)</rights><rights>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).</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4434-3a31ed5730df8ee1639b76c9b258f9ec99ce0da195a594ffff6c866dc6205d73</citedby><cites>FETCH-LOGICAL-c4434-3a31ed5730df8ee1639b76c9b258f9ec99ce0da195a594ffff6c866dc6205d73</cites><orcidid>0000-0002-0129-1079</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbmr.4274$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbmr.4274$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33666947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ish‐Shalom, Sofia</creatorcontrib><creatorcontrib>Caraco, Yoseph</creatorcontrib><creatorcontrib>Khazen, Nariman Saba</creatorcontrib><creatorcontrib>Gershinsky, Michal</creatorcontrib><creatorcontrib>Szalat, Auryan</creatorcontrib><creatorcontrib>Schwartz, Phillip</creatorcontrib><creatorcontrib>Arbit, Ehud</creatorcontrib><creatorcontrib>Galitzer, Hillel</creatorcontrib><creatorcontrib>Tang, Jonathan CY</creatorcontrib><creatorcontrib>Burshtein, Gregory</creatorcontrib><creatorcontrib>Rothner, Ariel</creatorcontrib><creatorcontrib>Raskin, Arthur</creatorcontrib><creatorcontrib>Blum, Miriam</creatorcontrib><creatorcontrib>Fraser, William D</creatorcontrib><title>Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study</title><title>Journal of bone and mineral research</title><addtitle>J Bone Miner Res</addtitle><description>ABSTRACT
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).</description><subject>25-Hydroxyvitamin D</subject><subject>Acetic acid</subject><subject>Adult</subject><subject>Adverse events</subject><subject>Calcitriol</subject><subject>Calcium</subject><subject>Calcium (blood)</subject><subject>Calcium (urinary)</subject><subject>Calcium phosphates</subject><subject>CALCIUM/PHOSPHATE DISORDERS</subject><subject>Dietary supplements</subject><subject>Dosage</subject><subject>Excretion</subject><subject>Humans</subject><subject>Hypercalciuria</subject><subject>Hyperphosphatemia</subject><subject>Hypocalcemia</subject><subject>HYPOPARATHYROIDISM</subject><subject>Hypoparathyroidism - drug therapy</subject><subject>Normocalcemia</subject><subject>ORAL PARATHYROID HORMONE</subject><subject>Original</subject><subject>Parathyroid</subject><subject>PARATHYROID HORMONE</subject><subject>Parathyroid Hormone - adverse effects</subject><subject>PARATHYROID‐RELATED DISORDERS</subject><subject>Quality of Life</subject><subject>Statistical analysis</subject><subject>Teriparatide - adverse effects</subject><issn>0884-0431</issn><issn>1523-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp10ctu1DAUBmALgehQWPACyBKbdpHW98QskErVMkWDBtHuLcd2qIfEDk4Cyo5H4Bn7JHiYtlwkvDkLf_p1jn4AnmN0hBEix5u6S0eMlOwBWGBOaMFEhR-CBaoqViBG8R54MgwbhJDgQjwGe5QKISQrF-DzpW7cOEMdLDxrGm-0mWFs4DrpFi6nTgf4QSc9Xs8peguXMXUxOHiAb77_oOwQ-gCXcx_738YP3St4EuC6dyGjla5dCy_Hyc5PwaNGt4N7djv3wdX52dXpslit316cnqwKwxhlBdUUO8tLimxTOYcFlXUpjKwJrxrpjJTGIaux5JpL1uQnTCWENYIgbku6D17vYvup7pw1Loz5GNUn3-k0q6i9-vsn-Gv1KX5VFeFEoCoHHNwGpPhlcsOoOj8Y17Y6uDgNijBZsbLkiGb68h-6iVMK-TpFOMOEC0lwVoc7ZVIchuSa-2UwUtsG1bZBtW0w2xd_bn8v7yrL4HgHvvnWzf9PUu_evP_4K_InQVCn5g</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>Ish‐Shalom, Sofia</creator><creator>Caraco, Yoseph</creator><creator>Khazen, Nariman Saba</creator><creator>Gershinsky, Michal</creator><creator>Szalat, Auryan</creator><creator>Schwartz, Phillip</creator><creator>Arbit, Ehud</creator><creator>Galitzer, Hillel</creator><creator>Tang, Jonathan CY</creator><creator>Burshtein, Gregory</creator><creator>Rothner, Ariel</creator><creator>Raskin, Arthur</creator><creator>Blum, Miriam</creator><creator>Fraser, William D</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TS</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0129-1079</orcidid></search><sort><creationdate>202106</creationdate><title>Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4434-3a31ed5730df8ee1639b76c9b258f9ec99ce0da195a594ffff6c866dc6205d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>25-Hydroxyvitamin D</topic><topic>Acetic acid</topic><topic>Adult</topic><topic>Adverse events</topic><topic>Calcitriol</topic><topic>Calcium</topic><topic>Calcium (blood)</topic><topic>Calcium (urinary)</topic><topic>Calcium phosphates</topic><topic>CALCIUM/PHOSPHATE DISORDERS</topic><topic>Dietary supplements</topic><topic>Dosage</topic><topic>Excretion</topic><topic>Humans</topic><topic>Hypercalciuria</topic><topic>Hyperphosphatemia</topic><topic>Hypocalcemia</topic><topic>HYPOPARATHYROIDISM</topic><topic>Hypoparathyroidism - drug therapy</topic><topic>Normocalcemia</topic><topic>ORAL PARATHYROID HORMONE</topic><topic>Original</topic><topic>Parathyroid</topic><topic>PARATHYROID HORMONE</topic><topic>Parathyroid Hormone - adverse effects</topic><topic>PARATHYROID‐RELATED DISORDERS</topic><topic>Quality of Life</topic><topic>Statistical analysis</topic><topic>Teriparatide - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ish‐Shalom, Sofia</creatorcontrib><creatorcontrib>Caraco, Yoseph</creatorcontrib><creatorcontrib>Khazen, Nariman Saba</creatorcontrib><creatorcontrib>Gershinsky, Michal</creatorcontrib><creatorcontrib>Szalat, Auryan</creatorcontrib><creatorcontrib>Schwartz, Phillip</creatorcontrib><creatorcontrib>Arbit, Ehud</creatorcontrib><creatorcontrib>Galitzer, Hillel</creatorcontrib><creatorcontrib>Tang, Jonathan CY</creatorcontrib><creatorcontrib>Burshtein, Gregory</creatorcontrib><creatorcontrib>Rothner, Ariel</creatorcontrib><creatorcontrib>Raskin, Arthur</creatorcontrib><creatorcontrib>Blum, Miriam</creatorcontrib><creatorcontrib>Fraser, William D</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bone and mineral research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ish‐Shalom, Sofia</au><au>Caraco, Yoseph</au><au>Khazen, Nariman Saba</au><au>Gershinsky, Michal</au><au>Szalat, Auryan</au><au>Schwartz, Phillip</au><au>Arbit, Ehud</au><au>Galitzer, Hillel</au><au>Tang, Jonathan CY</au><au>Burshtein, Gregory</au><au>Rothner, Ariel</au><au>Raskin, Arthur</au><au>Blum, Miriam</au><au>Fraser, William D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study</atitle><jtitle>Journal of bone and mineral research</jtitle><addtitle>J Bone Miner Res</addtitle><date>2021-06</date><risdate>2021</risdate><volume>36</volume><issue>6</issue><spage>1060</spage><epage>1068</epage><pages>1060-1068</pages><issn>0884-0431</issn><eissn>1523-4681</eissn><abstract>ABSTRACT
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).</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>33666947</pmid><doi>10.1002/jbmr.4274</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0129-1079</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 25-Hydroxyvitamin D Acetic acid Adult Adverse events Calcitriol Calcium Calcium (blood) Calcium (urinary) Calcium phosphates CALCIUM/PHOSPHATE DISORDERS Dietary supplements Dosage Excretion Humans Hypercalciuria Hyperphosphatemia Hypocalcemia HYPOPARATHYROIDISM Hypoparathyroidism - drug therapy Normocalcemia ORAL PARATHYROID HORMONE Original Parathyroid PARATHYROID HORMONE Parathyroid Hormone - adverse effects PARATHYROID‐RELATED DISORDERS Quality of Life Statistical analysis Teriparatide - adverse effects |
title | Safety and Efficacy of Oral Human Parathyroid Hormone (1‐34) in Hypoparathyroidism: An Open‐Label Study |
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