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Trial · NCT00365352

Results by group122

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in IRLS Rating Scale Total Score at Week 12 Using Last Observation Carried Forward (LOCF)Placebo-9.8Standard Deviation 7.69scores on a scale
Change From Baseline in IRLS Rating Scale Total Score at Week 12 Using Last Observation Carried Forward (LOCF)GEn (XP13512/GSK1838262) 1200 mg-13.0Standard Deviation 9.12scores on a scale
Number of Participants With a Score of Much Improved or Very Much Improved on the Investigator-rated CGI-I Scale (Response) at (Week 12) Using LOCFPlacebo43participants
Number of Participants With a Score of Much Improved or Very Much Improved on the Investigator-rated CGI-I Scale (Response) at (Week 12) Using LOCFGEn (XP13512/GSK1838262) 1200 mg86participants
Change From Baseline to the End of Treatment (Week 12) in the IRLS Rating Scale Total Score Using LOCFPlacebo-9.8Standard Deviation 7.69scores on a scale
Change From Baseline to the End of Treatment (Week 12) in the IRLS Rating Scale Total Score Using LOCFGEn (XP13512/GSK1838262) 600 mg-13.8Standard Deviation 8.09scores on a scale
Number of Participants Classsified as Responders on the Investigator-rated CGI-I Scale at Week 12 Using LOCFPlacebo43participants
Number of Participants Classsified as Responders on the Investigator-rated CGI-I Scale at Week 12 Using LOCFGEn (XP13512/GSK1838262) 600 mg83participants
Number of Participants Who Had an Onset of Response to Treatment at the End of Week 1 Based Upon the IRLS Rating Scale Total Score and the Investigator-rated CGI-I Using LOCFPlacebo13participants
Number of Participants Who Had an Onset of Response to Treatment at the End of Week 1 Based Upon the IRLS Rating Scale Total Score and the Investigator-rated CGI-I Using LOCFGEn (XP13512/GSK1838262) 600 mg36participants
Number of Participants Who Had an Onset of Response to Treatment at the End of Week 1 Based Upon the IRLS Rating Scale Total Score and the Investigator-rated CGI-I Using LOCFGEn (XP13512/GSK1838262) 1200 mg40participants
The Time to Onset of the First Response to Treatment on the IRLS Rating Scale Total Score and the Investigator-rated CGI-IPlaceboNA95% Confidence Interval NA to NAweeks
The Time to Onset of the First Response to Treatment on the IRLS Rating Scale Total Score and the Investigator-rated CGI-IGEn (XP13512/GSK1838262) 600 Milligrams(mg) Taken Orally4.195% Confidence Interval 2.1 to 8.1weeks
The Time to Onset of the First Response to Treatment on the IRLS Rating Scale Total Score and the Investigator-rated CGI-IGEn (XP13512/GSK1838262) 1200 mg Taken Orally Once a Day2.195% Confidence Interval 2.1 to 4.0weeks
Mean Change in the IRLS Rating Scale Total Score From Baseline at Week 12 by RLS Treatment History Using LOCFPlaceboNo RLS Treatment History-8.8Standard Deviation 7.08scores on a scale
Mean Change in the IRLS Rating Scale Total Score From Baseline at Week 12 by RLS Treatment History Using LOCFGEn (XP13512/GSK1838262) 600 mgNo RLS Treatment History-13.7Standard Deviation 8.23scores on a scale
Mean Change in the IRLS Rating Scale Total Score From Baseline at Week 12 by RLS Treatment History Using LOCFGEn (XP13512/GSK1838262) 1200 mgNo RLS Treatment History-12.5Standard Deviation 8.78scores on a scale
Mean Change in the IRLS Rating Scale Total Score From Baseline at Week 12 by RLS Treatment History Using LOCFPlaceboTreatment terminated-13.3Standard Deviation 9.09scores on a scale
Mean Change in the IRLS Rating Scale Total Score From Baseline at Week 12 by RLS Treatment History Using LOCFGEn (XP13512/GSK1838262) 600 mgTreatment terminated-12.4Standard Deviation 7.26scores on a scale
Mean Change in the IRLS Rating Scale Total Score From Baseline at Week 12 by RLS Treatment History Using LOCFGEn (XP13512/GSK1838262) 1200 mgTreatment terminated-17.1Standard Deviation 7.94scores 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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