Trial · NCT02969044
Results by group184
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 184
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 8 | PF-06651600 | Baseline | 45.15 | Standard Deviation 13.164 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 8 | Placebo | Baseline | 44.85 | Standard Deviation 13.976 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 8 | PF-06651600 | Change at Week 8 | -26.11 | Standard Deviation 14.834 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 8 | Placebo | Change at Week 8 | -17.38 | Standard Deviation 18.176 | units on a scale |
| Number of Participants With Vital Signs Abnormalities | PF-06651600 | Sitting DBP >=20 mmHg increase from baseline | 3 | Participants | |
| Number of Participants With Vital Signs Abnormalities | Placebo | Sitting DBP >=20 mmHg increase from baseline | 0 | Participants | |
| Number of Participants With Vital Signs Abnormalities | PF-06651600 | Sitting DBP >=20 mmHg decrease from baseline | 0 | Participants | |
| Number of Participants With Vital Signs Abnormalities | Placebo | Sitting DBP >=20 mmHg decrease from baseline | 1 | Participants | |
| Number of Participants With Laboratory Abnormalities | PF-06651600 | 42 | Participants | ||
| Number of Participants With Laboratory Abnormalities | Placebo | 28 | Participants | ||
| Number of Participants With Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs) | PF-06651600 | AEs | 20 | Participants | |
| Number of Participants With Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs) | Placebo | AEs | 5 | Participants | |
| Number of Participants With Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs) | PF-06651600 | SAEs | 0 | Participants | |
| Number of Participants With Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs) | Placebo | SAEs | 0 | Participants | |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 1, 2, 4 and 6 | PF-06651600 | Change at Week 1 | -4.59 | Standard Deviation 9.409 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 1, 2, 4 and 6 | Placebo | Change at Week 1 | -4.52 | Standard Deviation 7.025 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 1, 2, 4 and 6 | PF-06651600 | Change at Week 2 | -12.82 | Standard Deviation 10.969 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 1, 2, 4 and 6 | Placebo | Change at Week 2 | -8.05 | Standard Deviation 9.402 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 1, 2, 4 and 6 | PF-06651600 | Change at Week 4 | -17.79 | Standard Deviation 12.804 | units on a scale |
| Change From Baseline in Simple Disease Activity Index (SDAI) Score at Week 1, 2, 4 and 6 | Placebo | Change at Week 4 | -12.55 | Standard Deviation 13.462 | units 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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GET https://conductscience.org/api/trials/v1/NCT02969044/results