Randomized Teriparatide [Human Parathyroid Hormone (PTH) 1–34] Once-Weekly Efficacy Research (TOWER) Trial for Examining the Reduction in New Vertebral Fractures in Subjects with Primary Osteoporosis and High Fracture Risk
Context:Weekly teriparatide injection at a dose of 56.5 μg has been shown to increase bone mineral density.Objective:A phase 3 study was conducted to determine the efficacy of once-weekly teriparatide injection for reducing the incidence of vertebral fractures in patients with osteoporosis.Design an...
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Published in | The journal of clinical endocrinology and metabolism Vol. 97; no. 9; pp. 3097 - 3106 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda, MD
Oxford University Press
01.09.2012
Endocrine Society |
Subjects | |
Online Access | Get full text |
ISSN | 0021-972X 1945-7197 |
DOI | 10.1210/jc.2011-3479 |
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Abstract | Context:Weekly teriparatide injection at a dose of 56.5 μg has been shown to increase bone mineral density.Objective:A phase 3 study was conducted to determine the efficacy of once-weekly teriparatide injection for reducing the incidence of vertebral fractures in patients with osteoporosis.Design and Setting:In this randomized, multicenter, double-blind, placebo-controlled trial conducted in Japan, the incidence of morphological vertebral fractures by radiographs was assessed.Patients:Subjects were 578 Japanese patients between the ages of 65 and 95 yr who had prevalent vertebral fracture.Intervention:Subjects were randomly assigned to receive once-weekly sc injections of teriparatide (56.5 μg) or placebo for 72 wk.Main Outcome Measure:The primary endpoint was the incidence of new vertebral fracture.Results:Once-weekly injections of teriparatide reduced the risk of new vertebral fracture with a cumulative incidence of 3.1% in the teriparatide group, compared with 14.5% in the placebo group (P < 0.01), and a relative risk of 0.20 (95% confidence interval, 0.09 to 0.45). At 72 wk, teriparatide administration increased bone mineral density by 6.4, 3.0, and 2.3% at the lumbar spine, the total hip, and the femoral neck, respectively, compared with the placebo (P < 0.01). Adverse events (AE) and the dropout rates by AE were more frequently experienced in the teriparatide group, but AE were generally mild and tolerable.Conclusion:Weekly sc administration of teriparatide at a dose of 56.5 μg may provide another option of anabolic treatments in patients with osteoporosis at higher fracture risk. |
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AbstractList | Context:Weekly teriparatide injection at a dose of 56.5 μg has been shown to increase bone mineral density.Objective:A phase 3 study was conducted to determine the efficacy of once-weekly teriparatide injection for reducing the incidence of vertebral fractures in patients with osteoporosis.Design and Setting:In this randomized, multicenter, double-blind, placebo-controlled trial conducted in Japan, the incidence of morphological vertebral fractures by radiographs was assessed.Patients:Subjects were 578 Japanese patients between the ages of 65 and 95 yr who had prevalent vertebral fracture.Intervention:Subjects were randomly assigned to receive once-weekly sc injections of teriparatide (56.5 μg) or placebo for 72 wk.Main Outcome Measure:The primary endpoint was the incidence of new vertebral fracture.Results:Once-weekly injections of teriparatide reduced the risk of new vertebral fracture with a cumulative incidence of 3.1% in the teriparatide group, compared with 14.5% in the placebo group (P < 0.01), and a relative risk of 0.20 (95% confidence interval, 0.09 to 0.45). At 72 wk, teriparatide administration increased bone mineral density by 6.4, 3.0, and 2.3% at the lumbar spine, the total hip, and the femoral neck, respectively, compared with the placebo (P < 0.01). Adverse events (AE) and the dropout rates by AE were more frequently experienced in the teriparatide group, but AE were generally mild and tolerable.Conclusion:Weekly sc administration of teriparatide at a dose of 56.5 μg may provide another option of anabolic treatments in patients with osteoporosis at higher fracture risk. Weekly teriparatide injection at a dose of 56.5 μg has been shown to increase bone mineral density. A phase 3 study was conducted to determine the efficacy of once-weekly teriparatide injection for reducing the incidence of vertebral fractures in patients with osteoporosis. In this randomized, multicenter, double-blind, placebo-controlled trial conducted in Japan, the incidence of morphological vertebral fractures by radiographs was assessed. Subjects were 578 Japanese patients between the ages of 65 and 95 yr who had prevalent vertebral fracture. Subjects were randomly assigned to receive once-weekly s.c. injections of teriparatide (56.5 μg) or placebo for 72 wk. The primary endpoint was the incidence of new vertebral fracture. Once-weekly injections of teriparatide reduced the risk of new vertebral fracture with a cumulative incidence of 3.1% in the teriparatide group, compared with 14.5% in the placebo group (P < 0.01), and a relative risk of 0.20 (95% confidence interval, 0.09 to 0.45). At 72 wk, teriparatide administration increased bone mineral density by 6.4, 3.0, and 2.3% at the lumbar spine, the total hip, and the femoral neck, respectively, compared with the placebo (P < 0.01). Adverse events (AE) and the dropout rates by AE were more frequently experienced in the teriparatide group, but AE were generally mild and tolerable. Weekly s.c. administration of teriparatide at a dose of 56.5 μg may provide another option of anabolic treatments in patients with osteoporosis at higher fracture risk. Context:Weekly teriparatide injection at a dose of 56.5 mu g has been shown to increase bone mineral density.Objective:A phase 3 study was conducted to determine the efficacy of once-weekly teriparatide injection for reducing the incidence of vertebral fractures in patients with osteoporosis.Design and Setting:In this randomized, multicenter, double-blind, placebo-controlled trial conducted in Japan, the incidence of morphological vertebral fractures by radiographs was assessed.Patients:Subjects were 578 Japanese patients between the ages of 65 and 95 yr who had prevalent vertebral fracture.Intervention:Subjects were randomly assigned to receive once-weekly sc injections of teriparatide (56.5 mu g) or placebo for 72 wk.Main Outcome Measure:The primary endpoint was the incidence of new vertebral fracture.Results:Once-weekly injections of teriparatide reduced the risk of new vertebral fracture with a cumulative incidence of 3.1% in the teriparatide group, compared with 14.5% in the placebo group (P < 0.01), and a relative risk of 0.20 (95% confidence interval, 0.09 to 0.45). At 72 wk, teriparatide administration increased bone mineral density by 6.4, 3.0, and 2.3% at the lumbar spine, the total hip, and the femoral neck, respectively, compared with the placebo (P < 0.01). Adverse events (AE) and the dropout rates by AE were more frequently experienced in the teriparatide group, but AE were generally mild and tolerable.Conclusion:Weekly sc administration of teriparatide at a dose of 56.5 mu g may provide another option of anabolic treatments in patients with osteoporosis at higher fracture risk. |
Author | Shiraki, Masataka Nakamura, Toshitaka Hagino, Hiroshi Fukunaga, Masao Nishizawa, Yoshiki Ito, Masako Sugimoto, Toshitsugu Nakano, Tetsuo Kishimoto, Hideaki Fujita, Takuo Sone, Teruki Yoshikawa, Hideki |
Author_xml | – sequence: 1 givenname: Toshitaka surname: Nakamura fullname: Nakamura, Toshitaka email: toshinak@med.uoeh-u.ac.jp organization: 1Department of Orthopedic Surgery (T.Nakam.), University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan – sequence: 2 givenname: Toshitsugu surname: Sugimoto fullname: Sugimoto, Toshitsugu organization: 2Internal Medicine 1 (T.Su.), Shimane University Faculty of Medicine, Izumo 693-8501, Japan – sequence: 3 givenname: Tetsuo surname: Nakano fullname: Nakano, Tetsuo organization: 3Tamana Central Hospital (T.Nakan.), Tamana 865-0064, Japan – sequence: 4 givenname: Hideaki surname: Kishimoto fullname: Kishimoto, Hideaki organization: 4Sanin Rosai Hospital (H.K.), Yonago 683-8605, Japan – sequence: 5 givenname: Masako surname: Ito fullname: Ito, Masako organization: 5Division of Radiology (M.I.), Nagasaki University School of Medicine, Nagasaki 852-8501, Japan – sequence: 6 givenname: Masao surname: Fukunaga fullname: Fukunaga, Masao organization: 6Kawasaki Medical School (M.F.), Kurashiki 701-0192, Japan – sequence: 7 givenname: Hiroshi surname: Hagino fullname: Hagino, Hiroshi organization: 7School of Health Science & Rehabilitation Division (H.H.), Faculty of Medicine, Tottori University, Yonago 683-8503, Japan – sequence: 8 givenname: Teruki surname: Sone fullname: Sone, Teruki organization: 8Department of Radiology (T.So.), Division of Nuclear Medicine, Kawasaki Medical School, Kurashiki 701-0192, Japan – sequence: 9 givenname: Hideki surname: Yoshikawa fullname: Yoshikawa, Hideki organization: 9Department of Orthopedic Surgery (H.Y.), Osaka University Graduate School of Medicine, Suita 565-0871, Japan – sequence: 10 givenname: Yoshiki surname: Nishizawa fullname: Nishizawa, Yoshiki organization: 10Osaka City University (Y.N.), Osaka 558-8585, Japan – sequence: 11 givenname: Takuo surname: Fujita fullname: Fujita, Takuo organization: 11Katsuragi Hospital (T.F.), Kishiwada 590-0842, Japan – sequence: 12 givenname: Masataka surname: Shiraki fullname: Shiraki, Masataka organization: 12Research Institute and Practice for Involutional Diseases (M.S.), Azumino 399-8101, Japan |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26684655$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/22723322$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | Copyright © 2012 by The Endocrine Society 2012 2014 INIST-CNRS Copyright © 2012 by The Endocrine Society |
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Keywords | High risk Antiosteoporotic Peptide hormone Diseases of the osteoarticular system Vertebra Fracture Osteoarticular system Osteoporosis Osteoforming Randomization Reduction Weekly Scientific research Primary Clinical trial Nutritional status Human Obesity Nutrition Nutrition disorder Metabolic diseases Trauma Parathyroid hormone Endocrinology Teriparatide |
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PublicationTitle | The journal of clinical endocrinology and metabolism |
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SubjectTerms | Aged Aged, 80 and over Biological and medical sciences Bone Density Bone Density Conservation Agents - administration & dosage Bone Density Conservation Agents - adverse effects Bone Density Conservation Agents - therapeutic use Bone mineral density Double-Blind Method Endocrinopathies Endpoint Determination Feeding. Feeding behavior Female Fractures Fundamental and applied biological sciences. Psychology Humans Injections, Subcutaneous Japan Kaplan-Meier Estimate Male Medical sciences Osteoporosis Osteoporosis - complications Osteoporosis - diagnostic imaging Osteoporosis - prevention & control Parathyroid hormone Placebos Radiography Risk Reduction Behavior Spinal Fractures - diagnostic imaging Spinal Fractures - etiology Spinal Fractures - prevention & control Spine (lumbar) Spine - diagnostic imaging Survival Analysis Teriparatide - administration & dosage Teriparatide - adverse effects Teriparatide - therapeutic use Vertebrae Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: endocrinology |
Title | Randomized Teriparatide [Human Parathyroid Hormone (PTH) 1–34] Once-Weekly Efficacy Research (TOWER) Trial for Examining the Reduction in New Vertebral Fractures in Subjects with Primary Osteoporosis and High Fracture Risk |
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