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 inThe journal of clinical endocrinology and metabolism Vol. 97; no. 9; pp. 3097 - 3106
Main Authors Nakamura, Toshitaka, Sugimoto, Toshitsugu, Nakano, Tetsuo, Kishimoto, Hideaki, Ito, Masako, Fukunaga, Masao, Hagino, Hiroshi, Sone, Teruki, Yoshikawa, Hideki, Nishizawa, Yoshiki, Fujita, Takuo, Shiraki, Masataka
Format Journal Article
LanguageEnglish
Published Bethesda, MD Oxford University Press 01.09.2012
Endocrine Society
Subjects
Online AccessGet full text
ISSN0021-972X
1945-7197
DOI10.1210/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.
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
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Copyright © 2012 by The Endocrine Society
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Issue 9
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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Endocrine Society
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Snippet 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...
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...
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...
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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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