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OM202JP Clinical Study of KNP2002

A Phase II Clinical Study of KNP2002 Ointment in Patients With Common Warts (OM202JA)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05896215
Enrollment
159
Registered
2023-06-09
Start date
2023-06-12
Completion date
2024-07-27
Last updated
2024-09-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Common Wart

Keywords

Common Wart

Brief summary

The goal of this clinical trial is to evaluate safety and efficacy of KNP2002 in patients with common warts aged 15 to 50 years old.

Interventions

Dairy topical administration for 12 weeks

DRUGPlacebo of KNP2002

Dairy topical administration for 12 weeks

Sponsors

KinoPharma Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
15 Years to 49 Years
Healthy volunteers
No

Inclusion criteria

* Subjects aged 15 to 49 years old * Subjects with common warts on the upper or lower limb * Subjects who agree to contraception from obtaining consent to 4 weeks after the end of administration * Subjects who have given their voluntary written consent to participate in this clinical trial

Exclusion criteria

* Subjects with 5 or more warts on the upper or lower limbs * Subjects who are scheduled to undergo treatment such as physical therapy or chemotherapy for warts * Subjects with a history of allergy to topical skin preparations * Subjects with a history of malignant tumor within 5 years before administration of study drug * Subjects with any of the following diseases: Malignant tumor; Serious heart disease; Poorly controlled diabetes/hypertension * Women who are pregnant, may become pregnant, or are breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Change in wart areaAt 16 weeks after starting administrationPercent change in wart area from baseline

Secondary

MeasureTime frameDescription
Change in wart area over timeAt 4, 8, 12, and 16 weeks after starting administrationPercent change in wart area from baseline
Wart improvement rateAt 4, 8, 12, and 16 weeks after starting administrationWart improvement rate categorized by rate of change in wart area
Wart disappearance rateUp to 16 weeks after starting administrationProportion of patients with warts disappearing

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026