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Comparison · NCT02672111-deaths

CAM2038 q1w or q4w With Prior Exposure to SL BPN/NX vs CAM2038 q1w or q4w New to BPN Treatment: 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. CAM2038 q1w or q4w With Prior Exposure to SL BPN/NX vs CAM2038 q1w or q4w New to BPN Treatment: deaths from any cause. Trial comparisons, record NCT02672111-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02672111-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 1000.0198wilson
Risk in group 2000.0941wilson
Risk difference, group 1 minus group 20-0.09410.0198newcombe 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

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CAM2038 q1w or q4w With Prior Exposure to SL BPN/NXSubjects exposed to SL BPN/NX who received CAM2038 q1w or q4w0190EG000
Group 2CAM2038 q1w or q4w New to BPN TreatmentNew to BPN Treatment who received either CAM2028 q1w or q4w037EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Time frame of adverse events was 12 months - 48 weeks.

Source ClinicalTrials.gov

Trial

Title
Long-Term Safety Study of Buprenorphine (CAM2038) in Adult Outpatients With Opioid Use Disorder
NCT number
NCT02672111
Phases
PHASE3
Conditions
Opioid Use Disorder
Interventions
CAM2038 q1w or q4w exposure to SL BPN/NX, CAM2038 q1w or q4w new to BPN treatment
Lead sponsor
Braeburn Pharmaceuticals
Results first posted
2019-08-01

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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