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Comparison · NCT02979899-sae

TRC105 + Votrient vs Votrient: serious adverse events

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. TRC105 + Votrient vs Votrient: serious adverse events. Trial comparisons, record NCT02979899-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02979899-sae

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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 10.4290.3140.551wilson
Risk in group 20.2110.1250.333wilson
Risk difference, group 1 minus group 20.2180.05040.368newcombe hybrid score
Risk ratio, group 1 over group 22.041.143.63log
Odds ratio, group 1 over group 22.811.256.32log
Number needed to harm, for one more participant with a serious adverse event on TRC105 + Votrient than on Votrient4.592.7219.8from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TRC105 + VotrientAll patients that received at least one dose of TRC105 in combination with pazopanib2763EG000
Group 2VotrientAll patients that received at least one dose of pazopanib alone.1257EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were collected over the entire duration of the study (a period of 26 months).

Source ClinicalTrials.gov

Trial

Title
Trial of TRC105 and Pazopanib Versus Pazopanib Alone in Patients With Advanced Angiosarcoma
NCT number
NCT02979899
Phases
PHASE3
Conditions
Advanced Angiosarcoma
Interventions
TRC105, Votrient
Lead sponsor
Tracon Pharmaceuticals Inc.
Results first posted
2020-05-12

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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