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Comparison · NCT02970162-c42da1b1

Amifampridine Phosphate vs Placebo (for Amifampridine Phosphate): Triple Timed Up and Go Walk Test (3TUG)

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. Amifampridine Phosphate vs Placebo (for Amifampridine Phosphate): Triple Timed Up and Go Walk Test (3TUG). Trial comparisons, record NCT02970162-c42da1b1. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02970162-c42da1b1

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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 10.07690.01370.333wilson
Risk in group 20.6150.3550.823wilson
Risk difference, group 1 minus group 2-0.538-0.755-0.173newcombe hybrid score
Risk ratio, group 1 over group 20.1250.01810.862log
Odds ratio, group 1 over group 20.05210.005090.533log
Number needed to treat, for one fewer participant with the outcome on Amifampridine Phosphate than on Placebo (for Amifampridine Phosphate)1.861.325.77from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Amifampridine Phosphateamifampridine phosphate 10 mg (amifampridine equivalent) by mouth, 30 to 80 mg total daily dose, 3 to 4 times per day for 4 days~Amifampridine Phosphate113OG000
Group 2Placebo (for Amifampridine Phosphate)placebo by mouth 3 to 4 times per day for 4 days~Placebo Oral Tablet813OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Triple Timed Up and Go Walk Test (3TUG)
Description
The 3TUG is a functional mobility test that requires a patient to stand up from a straight-backed armchair, walk 3 meters, turn around, walk back, and sit down in the chair. A modification of this is where the individual performs the test 3 times without pause, and the measurement is the average time required to complete each of the 3 repetitions. Based upon literature reports that a significant change in gait for a similar walk-test is an increase in time of more than 20%, this has been incorporated into the endpoint.
Time frame
change from baseline in 3TUG at end of day 4
Population
The number and proportion of patients with a ≥20% increase in 3TUG average time

Source ClinicalTrials.gov

Trial

Title
Phase 3 Study to Evaluate Efficacy of Amifampridine Phosphate in Lambert-Eaton Myasthenic Syndrome (LEMS)
NCT number
NCT02970162
Phases
PHASE3
Conditions
Lambert-Eaton Myasthenic Syndrome
Interventions
Amifampridine Phosphate, Placebo Oral Tablet
Lead sponsor
Catalyst Pharmaceuticals, Inc.
Results first posted
2018-12-24

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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