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Trial · NCT03738150

Results by group26

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in Peak Oxygen Uptake (VO2 Max) at 24 WeeksSotatercept1.28Standard Deviation 2.628mL/min/kg
Change From Baseline in Right Ventricular Stroke Volume (RV SV) at 24 WeeksSotatercept-27.306Standard Deviation 26.5786mL
Change From Baseline in Right Ventricular End-Systolic Volume (RV ESV) at 24 WeeksSotatercept-39.151Standard Deviation 22.5544mL
Change From Baseline in Right Ventricular End-Diastolic Volume (RV EDV) at 24 WeeksSotatercept-66.459Standard Deviation 37.3311mL
Percent Change From Baseline in Right Ventricular Ejection Fraction (RV EF) at 24 WeeksSotatercept-1.3Standard Deviation 8.48Percent change
Change From Baseline in Right Ventricular Stroke Volume Index (RV SVI) at 24 WeeksSotatercept-15.073Standard Deviation 14.8219mL/m^2
Change From Baseline in Right Ventricular (RV) Mass at 24 WeeksSotatercept-6.240Standard Deviation 13.3558grams
Change From Baseline in Ventilatory Efficiency (VE/VCO2 Slope) at 24 WeeksSotatercept-8.87Standard Deviation 12.298Unitless
Change From Baseline in Cardiac Index at 24 WeeksSotatercept0.411Standard Deviation 1.1944Liter/min/m^2
Change From Baseline in Mean Pulmonary Arterial Pressure at 24 WeeksSotatercept-14.9Standard Deviation 13.22mmHg
Change From Baseline in Arteriovenous O2 Content Difference (Ca-vO2) at 24 WeeksSotatercept0.63Standard Deviation 2.131mL/100 mL
Change From Baseline in Pulmonary Vascular Resistance (PVR) at 24 WeeksSotatercept-305.728Standard Deviation 313.9827dynes*sec/cm^5
Change From Baseline in 6-Minute Walk Distance (6MWD) at 24 WeeksSotatercept66.35Standard Deviation 85.659meters
Change From Baseline in Concentration of Amino-Terminal Brain Natriuretic Propeptide (NT-proBNP) at 24 WeeksSotatercept-623.1Standard Deviation 840.56pg/mL
Change From Baseline in WHO (World Health Organization) Functional Class at 24 WeeksSotatercept-0.76Standard Deviation 0.903WHO functional class
Number of Participants With One or More Adverse Events (AEs)Sotatercept20Participants
Number of Participants Who Experienced One or More Events Indicative of Clinical Worsening of Pulmonary Arterial Hypertension (PAH)Sotatercept1Participants
Observed Trough Concentration (Ctrough) of Sotatercept at Cycle 9Sotatercept5884.79Standard Deviation 2933.77ng/mL
Maximum Plasma Concentration (Cmax) of Sotatercept at Cycle 9Sotatercept9732.785Standard Deviation 2852.373ng/mL
Minimum Plasma Concentration (Cmin) of Sotatercept at Cycle 9Sotatercept6234.303Standard Deviation 2466.046ng/mL

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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