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Trial · NCT02443688

Results by group85

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

OutcomeGroupCategoryValueSpreadUnits
Difference From Placebo in Absolute Change From Baseline in Forced Expiratory Volume in 1 Second Percent Predicted (ppFEV1)100 mg CTX-4430-1.3095% Confidence Interval -3.22 to 0.62FEV1 percent predicted
Difference From Placebo in Absolute Change From Baseline in Forced Expiratory Volume in 1 Second Percent Predicted (ppFEV1)50 mg CTX-4430-3.7695% Confidence Interval -5.65 to -1.86FEV1 percent predicted
Difference From Placebo in Absolute Change From Baseline in Forced Expiratory Volume in 1 Second Percent Predicted (ppFEV1)Pooled CTX-4430-2.5395% Confidence Interval -3.88 to -1.18FEV1 percent predicted
Difference From Placebo in Absolute Change From Baseline in Forced Expiratory Volume in 1 Second Percent Predicted (ppFEV1)Matching Placebo-2.6995% Confidence Interval -4.63 to -0.75FEV1 percent predicted
Number of Pulmonary Exacerbations Through 48 Weeks100 mg CTX-44301.5795% Confidence Interval 1.22 to 2.02pulmonary exacerbations per year
Number of Pulmonary Exacerbations Through 48 Weeks50 mg CTX-44301.4695% Confidence Interval 1.13 to 1.89pulmonary exacerbations per year
Number of Pulmonary Exacerbations Through 48 WeeksPooled CTX-44301.5195% Confidence Interval 1.26 to 1.81pulmonary exacerbations per year
Number of Pulmonary Exacerbations Through 48 WeeksMatching Placebo1.5695% Confidence Interval 1.21 to 2.01pulmonary exacerbations per year
Hazard Ratio Pulmonary Exacerbation While in the Study100 mg CTX-44300.8895% Confidence Interval 0.576 to 1.339hazard ratio
Hazard Ratio Pulmonary Exacerbation While in the Study50 mg CTX-44300.8695% Confidence Interval 0.563 to 1.308hazard ratio
Hazard Ratio Pulmonary Exacerbation While in the StudyPooled CTX-44300.8795% Confidence Interval 0.605 to 1.246hazard ratio
Subjects Without a Pulmonary Exacerbation While in the Study100 mg CTX-443025Participants
Subjects Without a Pulmonary Exacerbation While in the Study50 mg CTX-443026Participants
Subjects Without a Pulmonary Exacerbation While in the StudyPooled CTX-443051Participants
Subjects Without a Pulmonary Exacerbation While in the StudyMatching Placebo20Participants
Relative Change (Percent Change) From Baseline in ppFEV1100 mg CTX-4430-2.3895% Confidence Interval -5.37 to 0.60percent change from baseline
Relative Change (Percent Change) From Baseline in ppFEV150 mg CTX-4430-4.8195% Confidence Interval -7.84 to -1.79percent change from baseline
Relative Change (Percent Change) From Baseline in ppFEV1Pooled CTX-4430-3.6095% Confidence Interval -5.72 to -1.47percent change from baseline
Relative Change (Percent Change) From Baseline in ppFEV1Matching Placebo-3.4095% Confidence Interval -6.59 to -0.22percent change from baseline
Change From Baseline at 48 Weeks for Forced Vital Capacity Percent Predicted (FVC) and FEF25-75% (Forced Expiratory Flow During the Middle Half of the Forced Vital Capacity) Percent Predicted100 mg CTX-4430Forced vital capacity (FVC) percent predicted-1.5795% Confidence Interval -3.37 to 0.23absolute change of percent predicted

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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