Trial · NCT03597464
Results by group86
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 86
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | Any treatment-emergent adverse event (TEAE) | 100 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | Any treatment-emergent adverse event (TEAE) | 80 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | Treatment-related TEAE | 28 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | Treatment-related TEAE | 21 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | Serious TEAE | 21 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | Serious TEAE | 23 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | TEAE leading to study drug discontinuation | 11 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | TEAE leading to study drug discontinuation | 17 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | TEAE leading to death | 0 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | TEAE leading to death | 3 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | Treatment-related TEAE leading to death | 0 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | Treatment-related TEAE leading to death | 0 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | Disease-related TEAE | 50 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | Disease-related TEAE | 34 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Voclosporin | Disease-related serious TEAE | 7 | Participants | |
| Adverse Events (AE) Profile and Routine Biochemical and Hematological Assessments. | Placebo Oral Capsule | Disease-related serious TEAE | 11 | Participants | |
| Number (and Percent) of Subjects in Renal Response | Voclosporin | Renal Response - Month 12 | 61 | Participants | |
| Number (and Percent) of Subjects in Renal Response | Placebo Oral Capsule | Renal Response - Month 12 | 34 | Participants | |
| Number (and Percent) of Subjects in Renal Response | Voclosporin | Renal Response - Month 18 | 74 | Participants | |
| Number (and Percent) of Subjects in Renal Response | Placebo Oral Capsule | Renal Response - Month 18 | 46 | Participants |
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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