ConductScience.org, home

Comparison · NCT00525798-sae

SMC021 vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. SMC021 vs Placebo: serious adverse events. Trial comparisons, record NCT00525798-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00525798-sae

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1460.1320.161wilson
Risk in group 20.1620.1480.178wilson
Risk difference, group 1 minus group 2-0.0165-0.03720.00423newcombe hybrid score
Risk ratio, group 1 over group 20.8980.7851.03log
Odds ratio, group 1 over group 20.8810.7511.03log
Number needed to treat, for one fewer participant with a serious adverse event on SMC021 than on Placebo60.6from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1SMC0211 tablet of 0,80 mg SMC021 daily3402,334EG000
Group 2Placebo1 tablet of placebo daily3782,331EG001

Harm

What it counts
Total, serious adverse events
Time frame
From baseline to 36 month

Source ClinicalTrials.gov

Trial

Title
A Study to Evaluate Oral Salmon Calcitonin in the Treatment of Osteoporosis in Postmenopausal Women Taking Calcium and Vitamin D
NCT number
NCT00525798
Phases
PHASE3
Conditions
Osteoporosis
Interventions
SMC021 Oral calcitonin, SMC021 Placebo
Lead sponsor
Nordic Bioscience A/S
Results first posted
2012-10-18

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT00525798-sae