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	Pharmacodynamics (HPV Viral Load Assessment)	24 Weeks	Assessment of target lesions by quantitative PCR including HPV genotyping in swabs and biopsies
Primary	Pharmacodynamics (Local Immunity Status)	24 Weeks	Histological changes in immune cells in the mucosa/submucosa
Primary	Clinical Assessment (Lesions by RECIST)	24 Weeks	Efficacy assessment of lesions by RECIST
Primary	Clinical Assessment (Percent clearance of Lesions)	24 Weeks	Efficacy assessment of percent clearance of lesions
Primary	Clinical Assessment (Sum of the longest diameter (SLD))	24 Weeks	Efficacy assessment of the sum of the longest diameter (SLD))
Primary	Clinical Assessment (Histology)	24 Weeks	Efficacy assessment of the histology (regression of uVIN to no dysplasia)
Secondary	Safety and Tolerability (Adverse Events)	48 Weeks	Adverse Events will be collected throughout the study
Secondary	Safety and Tolerability (Laboratory Safety Testing)	48 Weeks	Laboratory Samples will be collected throughout the study
Secondary	Safety and Tolerability (12-Lead ECGs)	48 Weeks	12-Lead ECGs will be performed throughout the study
Secondary	Safety and Tolerability (Vital Signs)	48 Weeks	Vital Signs will be collected throughout the study
Secondary	Pharmacokinetics (Area Under the Curve)	12 Weeks	AUC will be computed
Secondary	Pharmacokinetics (Maximum Plasma Concentration)	12 Weeks	Cmax will be determined
Secondary	Pharmacokinetics (Tmax)	12 Weeks	Tmax will be determined

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/NCT02596074/registered