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Trial · NCT01433263

Results by group30

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

OutcomeGroupCategoryValueSpreadUnits
Percentage Change From Baseline of Thigh Muscle Volume (TMV) by MRI Scan at Week 830mg/kg BYM3382.0Standard Deviation 8.094Percentage Change of TMV
Percentage Change From Baseline of Thigh Muscle Volume (TMV) by MRI Scan at Week 8Placebo / Late 30mg/kg BYM3380.65Standard Deviation 8.239Percentage Change of TMV
Percentage Change in Body Weight From Baseline at Week 7 and Week 930mg/kg BYM338Week 7 (n= 15, 17)-3.3Standard Deviation 5.035Percent Change of Weight (kg)
Percentage Change in Body Weight From Baseline at Week 7 and Week 9Placebo / Late 30mg/kg BYM338Week 7 (n= 15, 17)-0.68Standard Deviation 4.457Percent Change of Weight (kg)
Percentage Change in Body Weight From Baseline at Week 7 and Week 930mg/kg BYM338Week 9 (n=14,16)-1.8Standard Deviation 7.131Percent Change of Weight (kg)
Percentage Change in Body Weight From Baseline at Week 7 and Week 9Placebo / Late 30mg/kg BYM338Week 9 (n=14,16)-0.32Standard Deviation 3.271Percent Change of Weight (kg)
Maximum Observed Serum Concentration (Cmax)30mg/kg BYM338422Standard Deviation 142ng/ml
Maximum Observed Serum Concentration (Cmax)Placebo / Late 30mg/kg BYM338408Standard Deviation 78.4ng/ml
Time to Reach the Maximum Concentration After Drug Administration (Tmax)30mg/kg BYM3382.05Inter-Quartile Range 142hr
Time to Reach the Maximum Concentration After Drug Administration (Tmax)Placebo / Late 30mg/kg BYM3382.22Inter-Quartile Range 78.4hr
Percentage Change From Baseline in Total Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) Compared to Placebo: at Week 830mg/kg BYM3384.97Standard Deviation 7.537Percentage Change in LBM
Percentage Change From Baseline in Total Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) Compared to Placebo: at Week 8Placebo / Late 30mg/kg BYM3382.41Standard Deviation 4.625Percentage Change in LBM
Percentage Change From Baseline of Bone Mineral Density (BMD) by Dual-Energy X-ray Absorptiometery (DXA) Compared to Placebo at Week 830mg/kg BYM3380.51Standard Deviation 3.712Percentage Change in BMD
Percentage Change From Baseline of Bone Mineral Density (BMD) by Dual-Energy X-ray Absorptiometery (DXA) Compared to Placebo at Week 8Placebo / Late 30mg/kg BYM3380.14Standard Deviation 4.14Percentage Change in BMD
Percentage Change From Baseline of Physical Activity Levels (Using the ActivPAL™ Device) Number of Steps Taken Compared to Placebo at Week 4 and 730mg/kg BYM338Week 4 (n=18, 23)917.78Standard Deviation 3720.491percentage change in number of steps
Percentage Change From Baseline of Physical Activity Levels (Using the ActivPAL™ Device) Number of Steps Taken Compared to Placebo at Week 4 and 7Placebo / Late 30mg/kg BYM338Week 4 (n=18, 23)63.59Standard Deviation 130.913percentage change in number of steps
Percentage Change From Baseline of Physical Activity Levels (Using the ActivPAL™ Device) Number of Steps Taken Compared to Placebo at Week 4 and 730mg/kg BYM338Week 7 (n=13, 22)-17.37Standard Deviation 80.350percentage change in number of steps
Percentage Change From Baseline of Physical Activity Levels (Using the ActivPAL™ Device) Number of Steps Taken Compared to Placebo at Week 4 and 7Placebo / Late 30mg/kg BYM338Week 7 (n=13, 22)35.80Standard Deviation 119.486percentage change in number of steps
Percentage Change From Baseline of Physical Activity Levels (Using the ActivPAL™ Device) Time Sedentary Taken Compared to Placebo at Week 4 and 730mg/kg BYM338Week 4 (n=18, 23)-0.05Standard Deviation 10.049percentage change in time (minutes)
Percentage Change From Baseline of Physical Activity Levels (Using the ActivPAL™ Device) Time Sedentary Taken Compared to Placebo at Week 4 and 7Placebo / Late 30mg/kg BYM338Week 4 (n=18, 23)52.25Standard Deviation 207.403percentage change in time (minutes)

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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