DRUG
"Teriparatide", "Forteo® or Teribon"
To examine the effects of terimaratide less than 6 months in osteoporosis
Status
Unknown
Phase
Phase 2
Enrollment
90
Locations
1
Results
Not posted
Publications
0
Study summary
The aim of this study is to examine the efficacy and adverse events in the following 3 groups in osteoporosis patients: 1. The administration period of teriparatide is less than 6 months and thereafter, denosumab for 24 months. 2. The administration period of teriparatide is from 6 to 12 months and thereafter, denosumab for 24 months. 3. The administration period of teriparatide is more than 12 months and thereafter, denosumab for 24 months.
Interventions
DRUG
To examine the effects of terimaratide less than 6 months in osteoporosis
Timeline
First posted
Oct 10, 2018
Study start
Oct 9, 2018
Primary completion
Oct 8, 2023
Study completion
Oct 8, 2025
Results posted
Not reported
Registry updated
Sep 21, 2021
Outcomes
Bone mineral density
Time frame · Change from Baseline Values at 1 year
Not reported in the indexed record.
Eligibility
Inclusion Criteria: * Osteoporotic patients who want to take teriparatide and denosumab Exclusion Criteria: * Patients who are allergic to teriparatide or denosumab Patients who are pregnant or breast-feedin
Study locations
Japan. Showing up to 24 locations stored in the fast local snapshot.
Yukio Nakamura
Matsumoto, Nagano, Japan
Publications
No PMID-linked publications were present in this registry snapshot.
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Related PeptideStat pages
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