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Trial · NCT01552681

Results by group116

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

OutcomeGroupCategoryValueSpreadUnits
Change From Screening in Stimulated Whole Salivary Flow at Week 24Baminercept 100 mg0.0Standard Deviation 0.3mL/min
Change From Screening in Stimulated Whole Salivary Flow at Week 24Placebo0.1Standard Deviation 0.2mL/min
Change From Screening in Stimulated Whole Salivary Flow at Week 48Baminercept 100 mg0.0Standard Deviation 0.3mL/min
Change From Screening in Stimulated Whole Salivary Flow at Week 48Placebo-0.1Standard Deviation 0.2mL/min
Change From Screening in Unstimulated Whole Salivary Flow at Week 24Baminercept 100 mg0.1Standard Deviation 0.2mL/min
Change From Screening in Unstimulated Whole Salivary Flow at Week 24Placebo0.1Standard Deviation 0.1mL/min
Change From Screening in Unstimulated Whole Salivary Flow at Week 48Baminercept 100 mg0.1Standard Deviation 0.1mL/min
Change From Screening in Unstimulated Whole Salivary Flow at Week 48Placebo0.1Standard Deviation 0.1mL/min
Change From Baseline in European League Against Rheumatism (EULAR) Sjogren's Syndrome Disease Activity Index (ESSDAI) at Week 24Baminercept 100 mg-1.1Standard Deviation 2.3units on a scale
Change From Baseline in European League Against Rheumatism (EULAR) Sjogren's Syndrome Disease Activity Index (ESSDAI) at Week 24Placebo-0.4Standard Deviation 3.1units on a scale
Percent of Subjects Classified as Responders According to the Patient Self-Assessment of Fatigue, Overall Dryness, and Joint Pain at Week 24Baminercept 100 mg20.7Percent of participants
Percent of Subjects Classified as Responders According to the Patient Self-Assessment of Fatigue, Overall Dryness, and Joint Pain at Week 24Placebo22.2Percent of participants
Percent of Subjects Classified as Responders According to the Patient Self-Assessment of Fatigue, Overall Dryness, and Joint Pain at Week 48Baminercept 100 mg21.4Percent of participants
Percent of Subjects Classified as Responders According to the Patient Self-Assessment of Fatigue, Overall Dryness, and Joint Pain at Week 48Placebo5.6Percent of participants
Change From Baseline in Visual Analog Scale (VAS) Scores for Sjogren's Syndrome Symptom Survey at Week 24Baminercept 100 mgDifficulty speaking due to dryness-0.7Standard Deviation 29.1mm
Change From Baseline in Visual Analog Scale (VAS) Scores for Sjogren's Syndrome Symptom Survey at Week 24PlaceboDifficulty speaking due to dryness-9.2Standard Deviation 18.6mm
Change From Baseline in Visual Analog Scale (VAS) Scores for Sjogren's Syndrome Symptom Survey at Week 24Baminercept 100 mgDifficulty swallowing due to dryness-6.5Standard Deviation 23.6mm
Change From Baseline in Visual Analog Scale (VAS) Scores for Sjogren's Syndrome Symptom Survey at Week 24PlaceboDifficulty swallowing due to dryness-10.1Standard Deviation 20.5mm
Change From Baseline in Visual Analog Scale (VAS) Scores for Sjogren's Syndrome Symptom Survey at Week 24Baminercept 100 mgDryness of mouth-11.4Standard Deviation 27.2mm
Change From Baseline in Visual Analog Scale (VAS) Scores for Sjogren's Syndrome Symptom Survey at Week 24PlaceboDryness of mouth-12.7Standard Deviation 23.1mm

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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