CANDIN
BiologicalCandida albicans Skin Test Antigen for Cellular Hypersensitivity
NCT Number: NCT02393417
This is a placebo-controlled, double-blind (subject, Investigator, and site staff with the exception of unblinded dedicated staff to handle study medication), phase 2a study with 3 dose cohorts, randomized (concealed) to CANDIN or placebo (3:1). Main study will be up to 20 weeks (10 doses administered every other week) or until a subject has complete resolution of all injectable common warts. Subjects who cannot tolerate dosing every 2 weeks due to a local tolerance issue may be injected at 3-week intervals for up to 10 doses, increasing the length of the study to 29 weeks. Subjects will be followed for 4 months after final injection(s) for evidence of new or reoccurring warts and for safety evaluation.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Johnson Dermatology, Fort Smith, Arkansas, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Candida albicans Skin Test Antigen for Cellular Hypersensitivity
0.9% Sodium Chloride Injection USP (non-preserved)
Time frame: 45 weeks
Complete resolution of a wart was defined as the absence of visible or measurable presence of the wart
Time frame: 45 weeks
Complete resolution of a wart was defined as the absence of visible or measurable presence of the wart
Time frame: 4 month follow up visit at 45 weeks
Complete resolution of a wart was defined as the absence of visible or measurable presence of the wart
Time frame: 45 weeks
Complete resolution of a wart was defined as the absence of visible or measurable presence of the wart
Time frame: 45 weeks
Time frame: 45 weeks
Time frame: 45 weeks
Scarring at any visit, many reports were transient being noted at only one or two visits and noted as resolving during the course of the study
Time frame: 45 weeks
Time frame: 45 weeks
Time frame: 45 weeks
Complete resolution of a wart was defined as the absence of visible or measurable presence of the wart
Time frame: 45 weeks
Time frame: 45 weeks
Complete resolution of a wart was defined as the absence of visible or measurable presence of the wart
Time frame: 45 weeks
Nielsen BioSciences, Inc.
Industry
A Phase IIa, Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of Varying Regimens of CANDIN for Treatment of Common Warts (Verruca Vulgaris)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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