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Trial · NCT02418000

Registered outcomes23

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
SecondaryNumber of Participants With Suppression of in pERK by PIA 24 Hours Post-doseCycle 1 Day 1, 24 hours post-dose.Blood assay: Plasma inhibitory assay (PIA) measuring pERK in blood at 24 hours post-dose
SecondaryNumber of Participants With Suppression of pFLT3 by PIA at 4 Hours Post-doseCycle 1 Day 1, 4 hours post-dose.Blood assay: Plasma inhibitory assay (PIA) measuring pFLT3 in blood at 4 hours post-dose
SecondaryNumber of Participants With Suppression of pFLT3 by PIA at 24 Hours Post-doseCycle 1 Day 1, 24 hours post-dose.Blood assay: Plasma inhibitory assay (PIA) measuring pFLT3 in blood at 24 hours post-dose

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT02418000/registered?page=2