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NCT03186378 · ClinicalTrials.gov registry record · Phase 2

Evaluation of Systemic Exposure to VP-102 in Subjects With Molluscum Contagiosum.

A Phase 2 study, sponsored by Verrica Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
33
Enrollment target

NCT03186378: Completed Phase 2 study, sponsored by Verrica Pharmaceuticals.

NCT03186378 is a Phase 2 study that has completed, run by Verrica Pharmaceuticals. The registered enrollment target is 33 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (75% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03186378, a Phase 2 study, has completed, sponsored by Verrica Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
33 participants
Enrollment target

Study Summary

The primary objective of the study is to determine the presence or absence of systemic cantharidin exposure from a single 24-hour dermal application of VP-102 topical film-forming solution \[0.7% (w/v) cantharidin\] (VP-102) when applied to molluscum contagiosum (molluscum) lesions on pediatric subjects 2 years old and older. Treatment will continue over the course of 3 additional 21 day intervals allowing for further evaluation of safety, efficacy and impact on quality of life.

Primary Outcome

The primary objective is to determine any potential systemic exposure from a single 24-hour dermal application of VP-102 topical film-forming solution when applied to molluscum contagiosum (molluscum) lesions on pediatric subjects 2 years old and older.

Interventions

  • COMBINATION_PRODUCT VP-102 with applicator

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2017-06-08
Est. Completion 2018-06-25
Phase Phase 2
Verrica Pharmaceuticals

9 total trials

What the finished NCT03186378 record still lists

NCT03186378 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (75% lower).

The record links to 0 conditions, and to 1 intervention - of which VP-102 with applicator is the first listed.

NCT03186378 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03186378 about?

NCT03186378 is a clinical study titled "Evaluation of Systemic Exposure to VP-102 in Subjects With Molluscum Contagiosum.". The primary objective of the study is to determine the presence or absence of systemic cantharidin exposure from a single 24-hour dermal application of VP-102 topical film-forming solution \[0.7% (w/v) cantharidin\] (VP-102) when applied to molluscum contagiosum (molluscum) lesions on pediatric subj...

What is the current status of trial NCT03186378?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 33 participants. The study started on 2017-06-08. Estimated completion is 2018-06-25.

What interventions are being tested in trial NCT03186378?

The interventions under investigation include: VP-102 with applicator (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT03186378?

This trial is sponsored by Verrica Pharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03186378's enrollment target sits among peer trials

33 1553rd of 2000 higher than 438 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03186378, the US trial registry maintained by the National Library of Medicine. NCT03186378 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.