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Comparison · NCT01795859-0fce3400

SD-809 Tablets vs SD-809 Placebo: Number of Participants With Treatment Success at the End of Therapy Based on Clinical Global Impression of Change (CGIC)

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

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

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ConductScience Library. SD-809 Tablets vs SD-809 Placebo: Number of Participants With Treatment Success at the End of Therapy Based on Clinical Global Impression of Change (CGIC). Trial comparisons, record NCT01795859-0fce3400. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01795859-0fce3400

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Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.4220.290.567wilson
Risk in group 20.1330.06260.262wilson
Risk difference, group 1 minus group 20.2890.1040.45newcombe hybrid score
Risk ratio, group 1 over group 23.171.47.19log
Odds ratio, group 1 over group 24.751.6713.5log
Number needed to treat, for one more participant with the outcome on SD-809 Tablets than on SD-809 Placebo3.462.229.59from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1SD-809 TabletsSD-809: SD-809 tablets are available in three dose strengths: 6, 9 and 12 mg, all of which are identical in size, shape and color (white).1945OG000
Group 2SD-809 PlaceboPlacebo: Placebo tablets are identical in appearance to SD-809 tablets.645OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Treatment Success at the End of Therapy Based on Clinical Global Impression of Change (CGIC)
Description
A treatment success is defined as Much or Very Much Improved at the Week 12 visit. The PGIC is a 7-point Likert Scale, ranging from very much worse to very much improved. The clinician was asked to comment about the subject.
Time frame
12 weeks
Population
The Modified ITT (mITT) Population was defined as all subjects in the ITT Population who received study drug and had at least one post-baseline assessment.

Source ClinicalTrials.gov

Trial

Title
First Time Use of SD-809 in Huntington Disease
NCT number
NCT01795859
Phases
PHASE3
Conditions
Chorea
Interventions
SD-809, Placebo
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Results first posted
2017-08-11

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.

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