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Trial · NCT03321617

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPOMA 40mg BID (80mg)03
Total, all-cause mortalityPOMA 80mg BID (160 mg)03
Total, all-cause mortalityPOMA 120mg BID (240mg)02
Total, all-cause mortalityPOMA 160 mg BID (320 mg)03
Total, other adverse eventsPOMA 40mg BID (80mg)13
Total, other adverse eventsPOMA 80mg BID (160 mg)33
Total, other adverse eventsPOMA 120mg BID (240mg)12
Total, other adverse eventsPOMA 160 mg BID (320 mg)23
Total, serious adverse eventsPOMA 40mg BID (80mg)03
Total, serious adverse eventsPOMA 80mg BID (160 mg)03
Total, serious adverse eventsPOMA 120mg BID (240mg)02
Total, serious adverse eventsPOMA 160 mg BID (320 mg)03

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/NCT03321617/event-totals