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Comparison · NCT02534844-86aba8e3

Adrabetadex vs Sham Control: Parts A/ B: Number of Participants Classified as CGIC Responders at Week 52

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. Adrabetadex vs Sham Control: Parts A/ B: Number of Participants Classified as CGIC Responders at Week 52. Trial comparisons, record NCT02534844-86aba8e3. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02534844-86aba8e3

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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 10.6050.4470.744wilson
Risk in group 20.3890.2030.614wilson
Risk difference, group 1 minus group 20.216-0.05850.448newcombe hybrid score
Risk ratio, group 1 over group 21.560.8262.93log
Odds ratio, group 1 over group 22.410.7637.61log
Number needed to treat, for one more participant with the outcome on Adrabetadex than on Sham Control4.62from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: sham.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1AdrabetadexParticipants received lumbar IT infusions of adrabetadex once every 2 weeks for a total of 52 weeks..2338OG001
Group 2Sham ControlParticipants received sham control procedures once every 2 weeks for a total of 52 weeks.718OG000

Outcome

Type
SECONDARY
Title
Parts A/ B: Number of Participants Classified as CGIC Responders at Week 52
Description
The Clinician CGIC is a 7-point Likert scale. The scale requires assessment of change from a baseline level of disease activity, with anchors ranging from markedly improved, moderately improved, and minimally improved to no change and corresponding worsening (minimally, moderately, markedly). The Investigator rates his/her impression of the change in each participant's condition at week 52 on a scale from marked improvement (1) to marked worsening (7). CGIC Responders are defined as participants who received the caregiver's rating of no change, minimally improved, moderately improved, or markedly improved from baseline to Week 52.
Time frame
Week 52
Population
mITT population included all randomized participants who received at least one treatment (sham or adrabetadex). As per planned analysis, efficacy data were collected and presented by overall randomized treatment assignment (either sham or adrabetadex). These two treatment arms (either sham or adrabetadex) combine data from Parts A and B of the study.

Source ClinicalTrials.gov

Trial

Title
VTS-270 to Treat Niemann-Pick Type C1 (NPC1) Disease
NCT number
NCT02534844
Phases
PHASE2, PHASE3
Conditions
Niemann-Pick Disease, Type C
Interventions
Parts A/B: Adrabetadex, Parts A/B: Sham Control
Lead sponsor
Mandos LLC
Results first posted
2023-02-22

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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