Examination of Efficacy and Safety of Other Anti-Resorption Drugs After 2-year-Denosumab Therapy in Japanese Osteoporosis Patients

  • End date
    Nov 23, 2026
  • participants needed
  • sponsor
    Shinshu University
Updated on 1 February 2022
denosumab therapy


The aim of this study is to examine the efficacy and adverse events in the following 3 groups in Japanese osteoporosis patients after 2-year-denosumab therapy:

SERM and eldecalcitol treatment for 24 months Bisphosphonates and eldecalcitol treatment for 24 months Eldecalcitol treatment for 24 months

Condition Osteoporosis
Treatment SERM "Viviant®Tablet 20mg" and ELD "Edirol®Tablet 0.75ug", Bisphosphonates and ELD "Edirol®Tablet 0.75ug", ELD "Edirol®Tablet 0.75ug"
Clinical Study IdentifierNCT03755193
SponsorShinshu University
Last Modified on1 February 2022


Yes No Not Sure

Inclusion Criteria

osteoporosis patients

Exclusion Criteria

not osteoporosis patients who are allergic to the drugs, refused to do this research, or who are pregnant
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