Trial · NCT02055157
Results by group150
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 150
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 1 | Subjects with at Least 1 Reported TEAE | 8 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 2 | Subjects with at Least 1 Reported TEAE | 8 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 3 | Subjects with at Least 1 Reported TEAE | 10 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 4 | Subjects with at Least 1 Reported TEAE | 9 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 1 | Subjects Least Reported Study Drug-Related TEAE | 7 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 2 | Subjects Least Reported Study Drug-Related TEAE | 8 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 3 | Subjects Least Reported Study Drug-Related TEAE | 9 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 4 | Subjects Least Reported Study Drug-Related TEAE | 9 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 1 | Subjects with at Least 1 Reported SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 2 | Subjects with at Least 1 Reported SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 3 | Subjects with at Least 1 Reported SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 4 | Subjects with at Least 1 Reported SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 1 | Subjects Least Reported Study Drug-Related SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 2 | Subjects Least Reported Study Drug-Related SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 3 | Subjects Least Reported Study Drug-Related SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 4 | Subjects Least Reported Study Drug-Related SAE | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 1 | Subjects Who Died | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 2 | Subjects Who Died | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 3 | Subjects Who Died | 0 | Participants | |
| Overall Summary of Adverse Events During Initial 6-Month Period | Cohort 4 | Subjects Who Died | 0 | 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.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT02055157/results