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RecruitingNCT03755193

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

Examination of Efficacy and Safety of SERM or Bisphosphonates After 2-year-Denosumab Therapy in Japanese Osteoporosis Patients

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Shinshu University · Academic / Other
Sex
All
Age
20 Years – 120 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGSERM "Viviant®Tablet 20mg" and ELD "Edirol®Tablet 0.75ug"To examine the effects of SERM and ELD in osteoporosis patients
DRUGBisphosphonates and ELD "Edirol®Tablet 0.75ug"To examine the effects of BP and ELD in osteoporosis patients
DRUGELD "Edirol®Tablet 0.75ug"To examine the effects of ELD in osteoporosis patients

Timeline

Start date
2018-11-24
Primary completion
2024-11-23
Completion
2026-11-23
First posted
2018-11-27
Last updated
2021-09-21

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT03755193. Inclusion in this directory is not an endorsement.

Examination of Efficacy and Safety of Other Anti-Resorption Drugs After 2-year-Denosumab Therapy in Japanese Osteoporosi (NCT03755193) · Clinical Trials Directory