ConductScience.org, home

Comparison · NCT05823012-d16ebe60

All Participants vs Participants Who Entered Maintenance Period: Proportion of Participants With Normalized TSH at End of Maintenance Period

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. All Participants vs Participants Who Entered Maintenance Period: Proportion of Participants With Normalized TSH at End of Maintenance Period. Trial comparisons, record NCT05823012-d16ebe60. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05823012-d16ebe60

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.6740.530.791wilson
Risk in group 20.7380.5890.847wilson
Risk difference, group 1 minus group 2-0.0642-0.2450.125newcombe hybrid score
Risk ratio, group 1 over group 20.9130.6971.2log
Odds ratio, group 1 over group 20.7330.2911.85log
Number needed to treat, for one fewer participant with the outcome on All Participants than on Participants Who Entered Maintenance Period15.6from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1All ParticipantsAll participants who received at least 1 dose of XP-8121 (100 to 1500 μg subcutaneous injection).3146OG000
Group 2Participants Who Entered Maintenance PeriodAll participants who received XP-8121 (100 to 1500 μg subcutaneous injection), completed the Titration Period, and entered the Maintenance Period.3142OG001

Outcome

Type
SECONDARY
Title
Proportion of Participants With Normalized TSH at End of Maintenance Period
Description
Proportion of participants enrolled with normalized TSH at the end of the Maintenance Period.
Time frame
Day 29 of the Maintenance Period
Population

Source ClinicalTrials.gov

Trial

Title
Study of XP-8121 For the Treatment of Adult Subjects With Hypothyroidism
NCT number
NCT05823012
Phases
PHASE2
Conditions
Hypothyroidism
Interventions
levothyroxine sodium
Lead sponsor
Xeris Pharmaceuticals
Results first posted
2025-07-03

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/NCT05823012-d16ebe60