ConductScience.org, home

Trial · NCT03033108

Results by group18

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

OutcomeGroupCategoryValueSpreadUnits
Change in Electrical Response of the Retina to a Flash of Light, as Measured by ElectroretinogramEmixustat Dose 1-12.23Full Range -41.0 to 54.7percent suppression
Change in Electrical Response of the Retina to a Flash of Light, as Measured by ElectroretinogramEmixustat Dose 268.00Full Range 1.0 to 91.5percent suppression
Change in Electrical Response of the Retina to a Flash of Light, as Measured by ElectroretinogramEmixustat Dose 396.69Full Range 64.9 to 100.0percent suppression
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 1Subjects with 1 or more adverse events6Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 2Subjects with 1 or more adverse events8Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 3Subjects with 1 or more adverse events6Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 1Subjects with 1 or more mild adverse events5Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 2Subjects with 1 or more mild adverse events5Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 3Subjects with 1 or more mild adverse events4Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 1Subjects with 1 or more moderate adverse events1Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 2Subjects with 1 or more moderate adverse events2Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 3Subjects with 1 or more moderate adverse events2Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 1Subjects with 1 or more severe adverse events0Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 2Subjects with 1 or more severe adverse events1Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 3Subjects with 1 or more severe adverse events1Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 1Subjects with 1 or more serious adverse events0Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 2Subjects with 1 or more serious adverse events0Participants
Percentage of Subjects With Adverse Events, by Severity and SeriousnessEmixustat Dose 3Subjects with 1 or more serious adverse events0Participants

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/NCT03033108/results