Trials / Recruiting
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
| Type | Name | Description |
|---|---|---|
| DRUG | SERM "Viviant®Tablet 20mg" and ELD "Edirol®Tablet 0.75ug" | To examine the effects of SERM and ELD in osteoporosis patients |
| DRUG | Bisphosphonates and ELD "Edirol®Tablet 0.75ug" | To examine the effects of BP and ELD in osteoporosis patients |
| DRUG | ELD "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.