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Comparison · NCT03095508-7762e440

Angal S (Arm A) vs ANTI-ANGIN® FORMULA (Arm B): Number of Participants Who Fully Recovered

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. Angal S (Arm A) vs ANTI-ANGIN® FORMULA (Arm B): Number of Participants Who Fully Recovered. Trial comparisons, record NCT03095508-7762e440. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03095508-7762e440

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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 10.930.8680.964wilson
Risk in group 20.930.8690.964wilson
Risk difference, group 1 minus group 2-0.00061-0.07150.07newcombe hybrid score
Risk ratio, group 1 over group 20.9990.9311.07log
Odds ratio, group 1 over group 20.9910.3592.74log
Number needed to treat, for one fewer participant with the outcome on Angal S (Arm A) than on ANTI-ANGIN® FORMULA (Arm B)1,640from 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 1Angal S (Arm A)
Patients received Angal S, topical spray \[Menthol\], 0,5 mg + 2 mg (Sandoz d.d., Slovenia), administered as three to five consecutive presses on the actuator button, 6-10 times per day, for a maximum 4 days or until full illness resolution
106114OG000
Group 2ANTI-ANGIN® FORMULA (Arm B)
Patients received ANTI-ANGIN® FORMULA, topical metered spray, 0,12 mg + 0,24 mg (LLC Valeant, Russia) administered as three to five consecutive presses on the actuator button, 6-10 times per day, for a maximum 4 days or until full illness resolution
107115OG001

Outcome

Type
SECONDARY
Title
Number of Participants Who Fully Recovered
Description
Number of Participants who Fully Recovered by Day 4 in Group A and by Day 5 in Group B (the outcome of a disease according to the objective evaluation by the Investigator, the total score according to the TSS questionnaire ≤ 2)
Time frame
Group A: 4 days Group B: 5 days
Population
ITT population

Source ClinicalTrials.gov

Trial

Title
Clinical Study for Comparative Assessment of Efficacy and Safety of Angal S, Topical Spray and ANTI-ANGIN® FORMULA, Topical Metered Spray in Treatment of Patients With Uncomplicated Acute Infectious and Inflammatory Diseases of the Pharynx, Accompanied by a Sore Throat
NCT number
NCT03095508
Phases
PHASE3
Conditions
Sore Throat
Interventions
Angal S, topical spray [Menthol], ANTI-ANGIN® FORMULA, topical metered spray
Lead sponsor
Sandoz
Results first posted
2019-03-21

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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