UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000056386 |
|---|---|
| Receipt number | R000064424 |
| Scientific Title | A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1 |
| Date of disclosure of the study information | 2025/02/01 |
| Last modified on | 2025/12/08 12:23:34 |
* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments
Basic information
Public title
A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1
Acronym
A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1
Scientific Title
A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1
Scientific Title:Acronym
A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1
Region
| Japan |
Condition
Condition
glucocorticoid-induced osteoporosis
Classification by specialty
| Clinical immunology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To compare the efficacy and safety of romosozumab and teriparatide in patients newly initiating glucocorticoid therapy
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
The percent change of bone mineral density of the lumbar spine (L2-4), femoral neck and total hip at 52 and 104 weeks in the romosozumab and teriparatide groups.
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -no one is blinded
Control
Active
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
Romosozumab group: Patients receive romosozumab subcutaneously. After 52 weeks of treatment, romosozumab will be discontinued and denosumab will be started. At week 156, final observation is performed.
Interventions/Control_2
Denosumab group: Patients receive teriparatide subcutaneously twice a week. After 104 weeks of treatment, teriparatide will be discontinued and denosumab will be started. At week 156, final observation is performed.
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 40 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
1) Patients 40 years of age or older newly initiating glucocorticoids, meeting the criteria for initiation of pharmacological therapy for glucocorticoid-induced osteoporosis
2) Patients who have provided written informed consent.
Key exclusion criteria
1) Patients with contraindications to romosozumab or denosumab.
2) Patients with active infection or malignancy.
3) Patients who are currently pregnant, lactating, or willing to get pregnant.
4) Patients who do not give consent to this study.
5) Patients previously treated with romosozumab or teriparatide
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | Mai |
| Middle name | |
| Last name | Kawazoe |
Organization
Toho University School of Medicine
Division name
Division of Rheumatology, Department of Internal Medicine
Zip code
143-8541
Address
6-11-1 Omori-nishi, Ota-ku, Tokyo
TEL
03-3762-4151
mai.kawazoe@med.toho-u.ac.jp
Public contact
Name of contact person
| 1st name | Mai |
| Middle name | |
| Last name | Kawazoe |
Organization
Toho University School of Medicine
Division name
Division of Rheumatology, Department of Internal Medicine
Zip code
143-8541
Address
6-11-1 Omori-nishi, Ota-ku, Tokyo
TEL
03-3462-4151
Homepage URL
mai.kawazoe@med.toho-u.ac.jp
Sponsor or person
Institute
Division of Rheumatology, Department of Internal Medicine, Toho University School of Medicine
Institute
Department
Personal name
Funding Source
Organization
Toho University School of Medicine
Division of Rheumatology, Department of Internal Medicine
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Toho University School of Medicine
Address
6-11-1 Omori-nishi, Ota-ku
Tel
03-3762-4151
mai.kawazoe@med.toho-u.ac.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2025 | Year | 02 | Month | 01 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Open public recruiting
Date of protocol fixation
| 2024 | Year | 12 | Month | 06 | Day |
Date of IRB
| 2025 | Year | 08 | Month | 06 | Day |
Anticipated trial start date
| 2025 | Year | 08 | Month | 26 | Day |
Last follow-up date
| 2030 | Year | 01 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2024 | Year | 12 | Month | 07 | Day |
Last modified on
| 2025 | Year | 12 | Month | 08 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064424
