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Trial · NCT03733444

Results by group167

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

OutcomeGroupCategoryValueSpreadUnits
Annual Rate of Decline in Forced Vital Capacity (FVC) up to Week 52GLPG1690, 600 mg-173.8Standard Error 18.04mL/year
Annual Rate of Decline in Forced Vital Capacity (FVC) up to Week 52GLPG1690, 200 mg-174.9Standard Error 17.65mL/year
Annual Rate of Decline in Forced Vital Capacity (FVC) up to Week 52Placebo-176.6Standard Error 17.74mL/year
Percentage of Participants With Disease Progression Up to 52 WeeksGLPG1690, 600 mg23.9Percentage of participants
Percentage of Participants With Disease Progression Up to 52 WeeksGLPG1690, 200 mg23.1Percentage of participants
Percentage of Participants With Disease Progression Up to 52 WeeksPlacebo22.1Percentage of participants
Percentage of Participants With Respiratory-Related Hospitalization Until End of Study (EoS)GLPG1690, 600 mg13.5Percentage of participants
Percentage of Participants With Respiratory-Related Hospitalization Until End of Study (EoS)GLPG1690, 200 mg10.8Percentage of participants
Percentage of Participants With Respiratory-Related Hospitalization Until End of Study (EoS)Placebo6.6Percentage of participants
Change From Baseline in St.George's Respiratory Questionnaire (SGRQ) Total Score at Week 52GLPG1690, 600 mg4.6Standard Error 1.13Score on a scale
Change From Baseline in St.George's Respiratory Questionnaire (SGRQ) Total Score at Week 52GLPG1690, 200 mg4.3Standard Error 1.08Score on a scale
Change From Baseline in St.George's Respiratory Questionnaire (SGRQ) Total Score at Week 52Placebo4.7Standard Error 1.10Score on a scale
Annual Rate of Decline of FVC Until EoSGLPG1690, 600 mg-179.5Standard Error 15.96mL/year
Annual Rate of Decline of FVC Until EoSGLPG1690, 200 mg-174.4Standard Error 15.63mL/year
Annual Rate of Decline of FVC Until EoSPlacebo-182.4Standard Error 15.72mL/year
Percentage of Participants With Disease Progression Until EoSGLPG1690, 600 mg31.7Percentage of participants
Percentage of Participants With Disease Progression Until EoSGLPG1690, 200 mg27.7Percentage of participants
Percentage of Participants With Disease Progression Until EoSPlacebo26.7Percentage of participants
Change From Baseline in St. George's Respiratory Questionnaire (SGRQ) Total Score at Week 100GLPG1690, 600 mg12.195% Confidence Interval 3.0 to 21.2Score on a scale
Change From Baseline in St. George's Respiratory Questionnaire (SGRQ) Total Score at Week 100GLPG1690, 200 mg14.895% Confidence Interval 4.6 to 25.1Score 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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