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Trial · NCT02958865

Results by group1,621

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

OutcomeGroupCategoryValueSpreadUnits
Total Mayo Score at Week 8 (Induction Period)Placebo (Induction)7.8890% Confidence Interval 6.95 to 8.81Units on a scale
Total Mayo Score at Week 8 (Induction Period)PF-06651600 20 mg (Induction)5.8590% Confidence Interval 5.18 to 6.51Units on a scale
Total Mayo Score at Week 8 (Induction Period)PF-06651600 70 mg (Induction)4.0090% Confidence Interval 3.33 to 4.67Units on a scale
Total Mayo Score at Week 8 (Induction Period)PF-06651600 200 mg (Induction)3.2790% Confidence Interval 2.58 to 3.96Units on a scale
Total Mayo Score at Week 8 (Induction Period)PF-06700841 10 mg (Induction)6.0890% Confidence Interval 5.43 to 6.74Units on a scale
Total Mayo Score at Week 8 (Induction Period)PF-06700841 30 mg (Induction)5.6090% Confidence Interval 4.93 to 6.27Units on a scale
Total Mayo Score at Week 8 (Induction Period)PF-06700841 60 mg (Induction)4.6790% Confidence Interval 4.01 to 5.33Units on a scale
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06651600 200 mg -> PF-06651600 50 mgParticipants with AEs18Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06651600 70 mg -> PF-06651600 50 mgParticipants with AEs27Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06651600 20 mg -> PF-06651600 50 mgParticipants with AEs18Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)Placebo -> PF-06651600 50 mgParticipants with AEs8Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06700841 60 mg -> PF-06700841 30 mgParticipants with AEs21Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06700841 30 mg -> PF-06700841 30 mgParticipants with AEs23Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06700841 10 mg -> PF-06700841 30 mgParticipants with AEs26Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)Placebo -> PF-06700841 30 mgParticipants with AEs4Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)Pooling Placebo During ChronicParticipants with AEs18Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06651600 200 mg -> PF-06651600 50 mgParticipants with SAEs3Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06651600 70 mg -> PF-06651600 50 mgParticipants with SAEs1Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)PF-06651600 20 mg -> PF-06651600 50 mgParticipants with SAEs1Participants
Number of Participants With AEs, SAEs and Discontinuation Due to AEs (Chronic Period)Placebo -> PF-06651600 50 mgParticipants with SAEs0Participants

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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