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Comparison · NCT00832091-421cc7d8

Thymosin Beta 4 (Tβ4) at 3 Doses vs Placebo: Wound Healing (Wound Closure Without Drainage) by Applying Tβ4 Gel Once Daily for up to 84 Days to Patients With Venous Stasis (VS) Ulcers

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. Thymosin Beta 4 (Tβ4) at 3 Doses vs Placebo: Wound Healing (Wound Closure Without Drainage) by Applying Tβ4 Gel Once Daily for up to 84 Days to Patients With Venous Stasis (VS) Ulcers. Trial comparisons, record NCT00832091-421cc7d8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00832091-421cc7d8

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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 10.2180.1290.344wilson
Risk in group 20.2350.09560.473wilson
Risk difference, group 1 minus group 2-0.0171-0.270.171newcombe hybrid score
Risk ratio, group 1 over group 20.9270.3442.5log
Odds ratio, group 1 over group 20.9070.253.3log
Number needed to treat, for one fewer participant with the outcome on Thymosin Beta 4 (Tβ4) at 3 Doses than on Placebo58.4from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Thymosin Beta 4 (Tβ4) at 3 Doses0.01% Tβ4 weight by weight (w/w), 0.03% Tβ4 w/w, 0.1% Tβ4 w/w1255OG001
Group 2Placebo0.00% Thymosin Beta 4 (Tβ4), weight/weight (w/w)417OG000

Outcome

Type
SECONDARY
Title
Wound Healing (Wound Closure Without Drainage) by Applying Tβ4 Gel Once Daily for up to 84 Days to Patients With Venous Stasis (VS) Ulcers
Description
Wound healing effectiveness of Tβ4 gel applied once daily for up to 84 days to patients expressed as the number of patients whose wound had closed without drainage at the end of the study, Day 84
Time frame
Up to 84 days
Population
Analysis per protocol, Intent-to-treat (ITT), using Last Observation Carried Forward (LOCF)

Source ClinicalTrials.gov

Trial

Title
Study of Thymosin Beta 4 in Patients With Venous Stasis Ulcers
NCT number
NCT00832091
Phases
PHASE2
Conditions
Venous Stasis Ulcers
Interventions
Thymosin Beta 4, Placebo
Lead sponsor
RegeneRx Biopharmaceuticals, Inc.
Results first posted
2010-03-24

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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