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Comparison · NCT02469857-7383a6de

Reltecimod (AB103) 0.5 mg/kg vs Placebo: Number of Deaths After Day 14 Through Day 90 Among Patients With a Screening mSOFA Score of at Least 5

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. Reltecimod (AB103) 0.5 mg/kg vs Placebo: Number of Deaths After Day 14 Through Day 90 Among Patients With a Screening mSOFA Score of at Least 5. Trial comparisons, record NCT02469857-7383a6de. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02469857-7383a6de

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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 10.04690.01610.129wilson
Risk in group 20.130.07020.23wilson
Risk difference, group 1 minus group 2-0.0836-0.1870.0183newcombe hybrid score
Risk ratio, group 1 over group 20.3590.1021.27log
Odds ratio, group 1 over group 20.3280.08461.27log
Number needed to treat, for one fewer participant with the outcome on Reltecimod (AB103) 0.5 mg/kg than on Placebo12from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Reltecimod (AB103) 0.5 mg/kgReltecimod 0.5 mg/kg, single IV infusion over approximately 10 minutes364OG000
Group 2PlaceboNaCl 0.9%, single IV infusion over approximately 10 minutes969OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Number of Deaths After Day 14 Through Day 90 Among Patients With a Screening mSOFA Score of at Least 5
Description
Number and percentage of patients with a Screening mSOFA score of at least 5 who were alive on Study Day 14 and subsequently died through Study Day 90.
Time frame
76 days (after Day 14 through Day 90)
Population
The United States modified intent-to-treat (US-mITT) population included all randomized patients in the United States who were exposed to study drug and who had a definitive diagnosis of NSTI based on surgical verification. This population does not include 17 patients randomized in France. Data from patients in the US-mITT population with a Screening mSOFA score of at least 5 who were alive on Day 14 (64 reltecimod patients and 69 placebo patients) were included in this analysis.

Source ClinicalTrials.gov

Trial

Title
Phase III Efficacy and Safety Study of AB103 in the Treatment of Patients With Necrotizing Soft Tissue Infections
NCT number
NCT02469857
Phases
PHASE3
Conditions
Necrotizing Soft Tissue Infections, Necrotizing Fasciitis, Fournier's Gangrene
Interventions
AB103 0.5 mg/kg, NaCl 0.9%
Lead sponsor
Atox Bio Ltd
Results first posted
2021-10-05

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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