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Trial · NCT03904693

Results by group56

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

OutcomeGroupCategoryValueSpreadUnits
Change in Pulmonary Vascular Resistance (PVR) Expressed as the Ratio of Geometric Means of End of Double-blind Treatment (EDBT) to BaselineDB: Treatment-naive And Prior ERA Strata: Macitentan Monotherapy 10 Milligrams (mg)0.7795% Confidence Interval 0.69 to 0.87Ratio
Change in Pulmonary Vascular Resistance (PVR) Expressed as the Ratio of Geometric Means of End of Double-blind Treatment (EDBT) to BaselineDB: Treatment-naive And Prior ERA Strata: M/T FDC0.5595% Confidence Interval 0.50 to 0.60Ratio
Change in Pulmonary Vascular Resistance (PVR) Expressed as the Ratio of Geometric Means of End of Double-blind Treatment (EDBT) to BaselineDB: Treatment-naive And Prior PDE-5i Strata: Tadalafil Monotherapy 20 mg (2 Tablets*20 mg)0.7895% Confidence Interval 0.72 to 0.84Ratio
Change in Pulmonary Vascular Resistance (PVR) Expressed as the Ratio of Geometric Means of End of Double-blind Treatment (EDBT) to BaselineDB: Treatment-naive And Prior PDE-5i Strata: M/T FDC0.5695% Confidence Interval 0.52 to 0.60Ratio
Change From Baseline to EDBT in 6-minutes Walking Distance (6MWD)DB: Treatment-naive And Prior ERA Strata: Macitentan 10 Milligrams (mg)38.5Standard Deviation 70.42Meters
Change From Baseline to EDBT in 6-minutes Walking Distance (6MWD)DB: Treatment-naive And Prior ERA Strata: M/T FDC52.9Standard Deviation 88.23Meters
Change From Baseline to EDBT in 6-minutes Walking Distance (6MWD)DB: Treatment-naive And Prior PDE-5i Strata: Tadalafil Monotherapy 20 mg (2 Tablets*20 mg)15.9Standard Deviation 45.04Meters
Change From Baseline to EDBT in 6-minutes Walking Distance (6MWD)DB: Treatment-naive And Prior PDE-5i Strata: M/T FDC43.4Standard Deviation 78.03Meters
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiopulmonary Symptom Domain Scores to EDBTDB: Treatment-naive And Prior ERA Strata: Macitentan 10 Milligrams (mg)-0.14Standard Deviation 0.478Score on a scale
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiopulmonary Symptom Domain Scores to EDBTDB: Treatment-naive And Prior ERA Strata: M/T FDC-0.20Standard Deviation 0.394Score on a scale
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiopulmonary Symptom Domain Scores to EDBTDB: Treatment-naive And Prior PDE-5i Strata: Tadalafil Monotherapy 20 mg (2 Tablets*20 mg)-0.13Standard Deviation 0.554Score on a scale
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiopulmonary Symptom Domain Scores to EDBTDB: Treatment-naive And Prior PDE-5i Strata: M/T FDC-0.15Standard Deviation 0.404Score on a scale
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiovascular Symptom Domain Scores to EDBTDB: Treatment-naive And Prior ERA Strata: Macitentan 10 Milligrams (mg)-0.14Standard Deviation 0.473Score on a scale
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiovascular Symptom Domain Scores to EDBTDB: Treatment-naive And Prior ERA Strata: M/T FDC-0.15Standard Deviation 0.349Score on a scale
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiovascular Symptom Domain Scores to EDBTDB: Treatment-naive And Prior PDE-5i Strata: Tadalafil Monotherapy 20 mg (2 Tablets*20 mg)-0.18Standard Deviation 0.612Score on a scale
Change From Baseline in Pulmonary Arterial Hypertension Symptoms and Impact (PAH-SYMPACT) in Cardiovascular Symptom Domain Scores to EDBTDB: Treatment-naive And Prior PDE-5i Strata: M/T FDC-0.10Standard Deviation 0.318Score on a scale
Percentage of Participants With Absence of Worsening in World Health Organization (WHO) Functional Class (FC) From Baseline at EDBTDB: Treatment-naive And Prior ERA Strata: Macitentan 10 Milligrams (mg)Stage: 1 : Class I5.60.590 to ?Percentage of participants
Percentage of Participants With Absence of Worsening in World Health Organization (WHO) Functional Class (FC) From Baseline at EDBTDB: Treatment-naive And Prior ERA Strata: M/T FDCStage: 1 : Class I5.30.561 to ?Percentage of participants
Percentage of Participants With Absence of Worsening in World Health Organization (WHO) Functional Class (FC) From Baseline at EDBTDB: Treatment-naive And Prior PDE-5i Strata: Tadalafil Monotherapy 20 mg (2 Tablets*20 mg)Stage: 1 : Class I4.50.522 to ?Percentage of participants
Percentage of Participants With Absence of Worsening in World Health Organization (WHO) Functional Class (FC) From Baseline at EDBTDB: Treatment-naive And Prior PDE-5i Strata: M/T FDCStage: 1 : Class I12.80.546 to ?Percentage of participants

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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