Trial · NCT03720886
G56W1 in Women With Postmenopausal Osteoporosis
NCT03720886, Phase 1, Phase 2, Unknown, Shenzhen Salubris Pharmaceuticals Co., Ltd.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. G56W1 in Women With Postmenopausal Osteoporosis. Trials, record NCT03720886. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03720886
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- G56W1 in Women With Postmenopausal Osteoporosis
- NCT number
- NCT03720886
- Status
- Unknown
- Phases
- Phase 1, Phase 2
- Enrollment
- 148 participants, estimated
- Lead sponsor
- Shenzhen Salubris Pharmaceuticals Co., Ltd.
- Conditions
- Postmenopausal Osteoporosis
- Interventions
- rhPTH（1-34） 28.2μg, rhPTH（1-34） 56.5μg, teriparatide acetate(Teribone™)
- First posted
- 2018-10-25
- Last updated
- 2018-10-25
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The percentage change in bone density of the lumbar spine ( L1-4 ) from baseline to 24 weeks after treatment | Baseline，week 24 | bone mineral density(BMD) measured by dual energy x-ray absorptiometry (DXA) |
| Secondary | Evaluate the rate of change of Procollagen I N-terminal peptide(PINP),Serum cross-linked C-terminal telopeptide of type I collagen(s-CTX) ,Bone alkaline phosphatase(BALP) , and blood calcium from baseline | Baseline，week 24 | Central lab will be used |
| Secondary | The percentage change of total hip bone density from baseline to 24 weeks after G56W1 treatment | Baseline，week 24 | BMD measured by DXA |
| Secondary | Maximum plasma concentration (Cmax) | Baseline，week 1，week 4，week 12，week 24 | serum parathyroid hormone(PTH) will be tested for all pharmacokinetics parameters |
| Secondary | Area under the plasma concentration versus time curve (AUC) | Baseline，week 1，week 4，week 12，week 24 | serum PTH will be tested for all pharmacokinetics parameters |
| Secondary | Time to maximum plasma concentration（Tmax） | Baseline，week 1，week 4，week 12，week 24 | serum PTH will be tested for all pharmacokinetics parameters |
| Secondary | Elimination half-life（t1/2） | Baseline，week 1，week 4，week 12，week 24 | serum PTH will be tested for all pharmacokinetics parameters |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03720886
GET https://conductscience.org/api/trials/v1/NCT03720886/registered