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Comparison · NCT02024087-812f435a

Dalantercept 0.4 mg/kg Plus Sorafenib vs Dalantercept 0.6 mg/kg Plus Sorafenib: Disease Control Rate (DCR)

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. Dalantercept 0.4 mg/kg Plus Sorafenib vs Dalantercept 0.6 mg/kg Plus Sorafenib: Disease Control Rate (DCR). Trial comparisons, record NCT02024087-812f435a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02024087-812f435a

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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 10.5330.3010.752wilson
Risk in group 20.6670.2080.939wilson
Risk difference, group 1 minus group 2-0.133-0.4910.375newcombe hybrid score
Risk ratio, group 1 over group 20.80.3162.03log
Odds ratio, group 1 over group 20.5710.04227.74log
Number needed to treat, for one fewer participant with the outcome on Dalantercept 0.4 mg/kg Plus Sorafenib than on Dalantercept 0.6 mg/kg Plus Sorafenib7.5from 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 1Dalantercept 0.4 mg/kg Plus SorafenibDalantercept plus sorafenib: Subcutaneous (SC) injection of dalantercept once every 3 weeks and oral sorafenib daily.815OG000
Group 2Dalantercept 0.6 mg/kg Plus SorafenibDalantercept plus sorafenib: Subcutaneous (SC) injection of dalantercept once every 3 weeks and oral sorafenib daily.23OG001

Outcome

Type
SECONDARY
Title
Disease Control Rate (DCR)
Description
Percentage of patients whose disease improves or remains stable over a certain time period. DCR is the sum of the complete, partial and stable disease rates.
Time frame
up to approximately 20 weeks
Population

Source ClinicalTrials.gov

Trial

Title
Study of Dalantercept and Sorafenib in Patients With Advanced Hepatocellular Carcinoma
NCT number
NCT02024087
Phases
PHASE1, PHASE2
Conditions
Advanced Adult Hepatocellular Carcinoma
Interventions
Dalantercept plus sorafenib
Lead sponsor
Acceleron Pharma, Inc., a wholly-owned subsidiary of Merck & Co., Inc., Rahway, NJ USA
Results first posted
2020-12-22

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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