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Comparison · NCT02514824-deaths

Dose Level 1: MLN01283 3 mg (Phase 1) vs Dose Level 2: MLN01283 4 mg (Phase 1): 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. Dose Level 1: MLN01283 3 mg (Phase 1) vs Dose Level 2: MLN01283 4 mg (Phase 1): deaths from any cause. Trial comparisons, record NCT02514824-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02514824-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 10.750.3010.954wilson
Risk in group 20.60.2310.882wilson
Risk difference, group 1 minus group 20.15-0.3810.572newcombe hybrid score
Risk ratio, group 1 over group 21.250.5023.11log
Odds ratio, group 1 over group 220.11235.8log
Number needed to harm, for one more death from any cause on Dose Level 1: MLN01283 3 mg (Phase 1) than on Dose Level 2: MLN01283 4 mg (Phase 1)6.67from 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 1Dose Level 1: MLN01283 3 mg (Phase 1)
Phase 1 dose level 1 participants receive MLN01283 3mg orally once daily of a 28 day cycle.~Participants are treated indefinitely until disease progression, unacceptable toxicity or withdrawal for other reasons.
34EG000
Group 2Dose Level 2: MLN01283 4 mg (Phase 1)
Phase 1 dose level 2 participants receive MLN01283 4 mg orally once daily of a 28 day cycle.~Participants are treated indefinitely until disease progression, unacceptable toxicity or withdrawal for other reasons.
35EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Assessed on treatment and for this study cohort the longest treatment duration was approximately 4 months in each dose level 1 and 2.

Source ClinicalTrials.gov

Trial

Title
MLN0128 in Recurrent/Metastatic Merkel Cell Carcinoma
NCT number
NCT02514824
Phases
PHASE1, PHASE2
Conditions
Merkel Cell Carcinoma
Interventions
MLN0128
Lead sponsor
Dana-Farber Cancer Institute
Results first posted
2020-12-29

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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