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Trial · NCT02943239

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryIncidence and severity of treatment-emergent adverse events (TEAEs)Up to 40 weeks
SecondaryPercent change in thigh muscle volume as measured by MRIUp to 28 weeks
SecondaryChange in thigh muscle volume as measured by MRIUp to 28 weeks
SecondaryPercent change in total and regional body composition as measured by Dual X-ray absorptiometry (DXA)Up to 28 weeks
SecondaryChange in total body composition as measured by DXAUp to 28 weeks
SecondaryChange in regional body composition as measured by DXAUp to 28 weeks
SecondaryPharmacokinetic profile of REGN2477 assessed via measurement of concentrations of REGN2477 in serum over timeUp to 40 weeks
SecondaryPharmacokinetic profile of REGN1033 assessed via measurement of concentrations of REGN1033 in serum overtimeUp to 40 weeks
SecondaryChange in total Activin A levels in bloodUp to 40 weeks
SecondaryChange in total GDF8 levels in bloodUp to 32 weeks
SecondaryPresence or absence of antibodies against REGN2477 and REGN1033Up to 40 weeks

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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GET https://conductscience.org/api/trials/v1/NCT02943239/registered