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Trial · NCT04138277

Results by group126

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Continued GroupSubjects with TEAEs80Participants
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Switched GroupSubjects with TEAEs37Participants
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Continued GroupSubjects with TESAEs17Participants
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Switched GroupSubjects with TESAEs10Participants
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Continued GroupSubjects with TEAEs leading to discontinuation6Participants
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Switched GroupSubjects with TEAEs leading to discontinuation2Participants
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Continued GroupSubjects with TEAE leading to death1Participants
Incidence of Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and TEAEs Leading to Discontinuation of Study DrugTreatment Switched GroupSubjects with TEAE leading to death0Participants
Change From Baseline in 6-Minute Walk Distance (6MWD)Treatment Continued Group-33.3Standard Deviation 37.60meters
Change From Baseline in 6-Minute Walk Distance (6MWD)Treatment Switched Group-8.6Standard Deviation 62.77meters
Change From Baseline in Sitting % Predicted Forced Vital Capacity (FVC)Treatment Continued Group-3.8Standard Deviation 9.10percent predicted FVC
Change From Baseline in Sitting % Predicted Forced Vital Capacity (FVC)Treatment Switched Group-0.5Standard Deviation 8.54percent predicted FVC
Change From Baseline in Manual Muscle Testing (MMT) Lower Extremity ScoreTreatment Continued Group0.6Standard Deviation 4.38score on a scale
Change From Baseline in Manual Muscle Testing (MMT) Lower Extremity ScoreTreatment Switched Group0.4Standard Deviation 2.61score on a scale
Change From Baseline in the Total Score for Patient-reported Outcomes Measurement Information System (PROMIS®) - Physical FunctionTreatment Continued Group-2.7Standard Deviation 8.38score on a scale
Change From Baseline in the Total Score for Patient-reported Outcomes Measurement Information System (PROMIS®) - Physical FunctionTreatment Switched Group-2.5Standard Deviation 6.14score on a scale
Change From Baseline in the Total Score for PROMIS® - FatigueTreatment Continued Group1.5Standard Deviation 7.14score on a scale
Change From Baseline in the Total Score for PROMIS® - FatigueTreatment Switched Group1.1Standard Deviation 3.72score on a scale
Change From Baseline in Gait, Stairs, Gower, Chair (GSGC) TestTreatment Continued Group0.5Standard Deviation 2.98score on a scale
Change From Baseline in Gait, Stairs, Gower, Chair (GSGC) TestTreatment Switched Group0.3Standard Deviation 1.59score on a scale

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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