Clinical trial · Interventional
Safety and Efficacy of Repeat Use of Picato® 0.05% in the Treatment of Anogenital Warts
NCT02377999CI-TRIAL-00086378completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
An exploratory open label, single treatment trial of anogenital warts with Picato® repeated up to 2 times with two weeks intervals.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Anogenital Warts | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Picato | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment of genetial warts with Picato
- interventionNames
- Drug: Picato
Primary outcomes (1)
- measure
- Number of incidence and severity of Local Skin Reactions (LSR)
- timeFrame
- Measured two weeks after every treatment and final measurement 2 weeks after last treatment
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * 1\. A clinical diagnosis of external anogenital/perianal warts with at least 2 warts and no more than 20 warts located in one or more of the following anatomic locations: 1. In both sexes: inguinal, perineal, and perianal areas 2. In men: penis shaft, scrotum, glans penis and foreskin 3. In women: on the vulva * 2\. Subjects has a total wart areas of at least 10 mm2, but not more than 500 mm2 * 3\. Female subjects of childbearing potential must be confirmed not pregnant by a negative urine pregnancy test prior to trial treatment Exclusion Criteria: * 1\. Subject has received any topical and/or destructive treatments for external anogenital warts within 4 weeks (within 12 months for imiquimod and within 12 weeks for sinecatechins) prior to enrolment * 2\. Subject suffer from any of the following conditions: 1. Known human immunodeficiency virus (HIV) infection 2. An outbreak of herpes genitalis in the wart areas within 4 weeks prior to enrolment 3. Has internal (rectal urethral, vaginal/cervical) warts that require or are undergoing treatment 4. Has a dermatological disease (e.g. psoriasis) or skin condition in the wart areas * 3\. Subjects using systemic virostatic compounds or immunosuppressive medication within 30 days prior to enrollment * 4\. Prior quadrivalent HPV vaccination
References
Publications (0)
Data not yet available
No reference posted for this study.