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Comparison · NCT03440814-deaths

DCCR vs Placebo for DCCR: deaths from any cause

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. DCCR vs Placebo for DCCR: deaths from any cause. Trial comparisons, record NCT03440814-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03440814-deaths

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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 1000.0437wilson
Risk in group 2000.0838wilson
Risk difference, group 1 minus group 20-0.08380.0437newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1DCCR
Participants with PWS were dosed dependent on their weight; 25mg, 75mg or 150mg DCCR tablets could be taken; DCCR was taken daily. Tablets must be swallowed whole and should not be broken, crushed or chewed.~The target dose by weight (kg) was as follows:~Subjects weighing 20 to \< 30 kg took 100mg DCCR/day; Subjects weighing ≥ 30 to \< 40 took 150mg DCCR/day; Subjects weighing ≥ 40 to \< 65 took 225mg DCCR/day; Subjects weighing ≥ 65 to \< 100 took 375mg DCCR/day; Subjects weighing ≥ 100 to \< 135 took 450mg DCCR/day. Subjects randomized to the DCCR treatment group were titrated every 2 weeks until the target dose was achieved.
084EG000
Group 2Placebo for DCCR
Participants with PWS were dosed dependent on their weight; 25mg, 75mg or 150mg placebo for DCCR tablets could be taken; Placebo was taken daily. Tablets must be swallowed whole and should not be broken, crushed or chewed.~The target dose by weight (kg) was as follows:~Subjects weighing 20 to \< 30 kg took 100mg DCCR/day; Subjects weighing ≥ 30 to \< 40 took 150mg DCCR/day; Subjects weighing ≥ 40 to \< 65 took 225mg DCCR/day; Subjects weighing ≥ 65 to \< 100 took 375mg DCCR/day; Subjects weighing ≥ 100 to \< 135 took 450mg DCCR/day. Subjects randomized to the Placebo group were titrated on placebo, similar to the DCCR group.
042EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Baseline to Visit 7 (Week 13)

Source ClinicalTrials.gov

Trial

Title
A Study of Diazoxide Choline in Patients With Prader-Willi Syndrome
NCT number
NCT03440814
Phases
PHASE3
Conditions
Prader-Willi Syndrome
Interventions
DCCR, Placebo for DCCR
Lead sponsor
Soleno Therapeutics, Inc.
Results first posted
2023-09-21

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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