Registered outcomes13

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

1 to 13 of 13

List	Outcome	Time frame	Description
Primary	Cmax	up to 48 hours post-dose	Primary PK parameters
Primary	AUC0-t	up to 48 hours post-dose	Primary PK parameters
Primary	AUC0-∞	up to 48 hours post-dose	Primary PK parameters
Primary	Tmax	up to 48 hours post-dose	Secondary PK parameters
Primary	Tlag	up to 48 hours post-dose	Secondary PK parameters
Primary	AUC0-4	up to 48 hours post-dose	Secondary PK parameters
Primary	AUC4-t	up to 48 hours post-dose	Secondary PK parameters
Primary	t1/2	up to 48 hours post-dose	Secondary PK parameters
Primary	λz	up to 48 hours post-dose	Secondary PK parameters
Primary	AUC_%Extrap	up to 48 hours post-dose	Secondary PK parameters
Primary	CL/F	up to 48 hours post-dose	Secondary PK parameters
Primary	VZ/F	up to 48 hours post-dose	Secondary PK parameters
Secondary	Incidence of adverse events (AEs) during the study	Through study completion, an average of 21 days

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

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT07897240/registered