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Trial record 2 of 3 for:    Recruiting Studies | Molluscum Contagiosum

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

This study is currently recruiting participants.
Verified June 2017 by Verrica Pharmaceuticals Inc.
Sponsor:
ClinicalTrials.gov Identifier:
NCT03186378
First Posted: June 14, 2017
Last Update Posted: June 15, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Collaborators:
Paidion Research, Inc
Database Integrations
Cato Research
Instat services
Information provided by (Responsible Party):
Verrica Pharmaceuticals Inc.
  Purpose
The primary objective of the study is to determine the systemic presence or absence of VP-102 topical film forming solution when applied to molluscum contagiosum lesions in subjects 2 years of age or older from a single 24-hour dermal application. 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.

Condition Intervention Phase
Molluscum Contagiosum Drug: VP-102 Device: VP-102 Applicator Phase 2

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Intervention Model Description:
Open label
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 2, Open-Label Study to Evaluate the Safety, Efficacy and Systemic Exposure of VP-102 Topical Film Forming Solution [0.7% (w/v) in Subjects (2 Years and Older) With Molluscum Contagiosum

Further study details as provided by Verrica Pharmaceuticals Inc.:

Primary Outcome Measures:
  • Systemic Exposure [ Time Frame: 24 hours ]
    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.


Secondary Outcome Measures:
  • Safety [ Time Frame: 12-14 weeks ]
    To assess the safety of VP-102, when applied to molluscum lesions on subjects 2 years old and older by assessing severity of local skin reactions such as erythema, blisters, or pain in response to treatment.

  • Efficacy [ Time Frame: 12-14 weeks ]
    To assess the efficacy of VP-102 in the treatment of molluscum lesions as assessed by clearance or reduction of treated molluscum lesions as compared to baseline.

  • Impact on Quality of Life [ Time Frame: 12-14 weeks ]
    To assess the impact of VP-102 treatment on quality of life of patients as assessed via the administration of the Children's Dermatology Life Quality Index (CDLQI).


Estimated Enrollment: 30
Actual Study Start Date: June 8, 2017
Estimated Study Completion Date: February 28, 2018
Estimated Primary Completion Date: January 31, 2018 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Exposure Group
This group is open label and allows for up to 16 subjects with 21 or more molluscum lesions will be enrolled. They must complete all blood draws or will be replaced. Intervention Drug: They will receive treatment to their molluscum contagiosum lesions per protocol with VP-102 using the VP-102 applicator.
Drug: VP-102
Subjects will receive treatment to their molluscum contagiosum with VP-102.
Device: VP-102 Applicator
The product is being considered by FDA as a combination therapy which includes the drug VP-102 and the applicator which is the device.
Experimental: Standard Group
This group is open label allowing up to 6 subjects with 20 lesions or less to be enrolled. This is to support those subjects that may have qualified at screening but due to a decrease in the number of lesions may not qualify on the treatment day. Intervention- Drug: These subjects will receive treatment to their molluscum lesions with VP-102 using the VP-102 applicator.
Drug: VP-102
Subjects will receive treatment to their molluscum contagiosum with VP-102.
Device: VP-102 Applicator
The product is being considered by FDA as a combination therapy which includes the drug VP-102 and the applicator which is the device.

Detailed Description:
This is a Phase 2, Open-Label Study to Evaluate the Safety, Efficacy and Systemic Exposure of VP-102 Topical Film Forming Solution in subjects 2 years and older with Molluscum Contagiosum. Up to 30 subjects with 21 or more lesions will be enrolled in the study. Subjects that do not have enough molluscum lesions to participate in the exposure study but do meet all other criteria to participate will be enrolled in a standard treatment group which will not require blood draws. No more than 16 subjects will complete exposure group activities; no more than 6 subjects will be enrolled in the standard treatment group. All subjects will be treated with VP-102 applied to their molluscum lesions every 21 days for a maximum of 4 sessions or until complete clearance. In the exposure group, blood samples for systemic exposure evaluation will be collected at designated intervals on Day 1 over a 24 hour period. A dermatologic examination will be performed by a qualified investigator quantifying molluscum lesion counts at every study visit.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   2 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Be healthy subjects ages 2 years and older.
  2. Patients with 1-20 lesions may be enrolled and treated in the standard treatment group but are not eligible for the exposure study.
  3. Patients with 21 or more lesions may only be enrolled in the exposure group. Subjects participating in the Exposure group must have at least 21 lesions treated at Day 1 to qualify.
  4. Be otherwise medically healthy with no clinically significant medical history as determined by the investigator. Patients exhibiting active Atopic Dermatitis may be enrolled.
  5. Refrain from application of all topical agents including alcohol-based sanitary products and sunscreens for a minimum of 4 hours before Study drug application. Topical agents including alcohol-based sanitary products and sunscreens may be used after application of the study drug so long as they are not applied to or near treated skin.
  6. Refrain from swimming, bathing or prolonged immersion in water until the Study drug is removed.
  7. Have the ability or have a guardian able to follow study instructions and be likely to complete all study requirements.
  8. Provide assent in a manner approved by the institutional review board (IRB) and have a parent/guardian provide written informed consent as evidenced by signature on IRB approved assent/consent forms.
  9. Provide written authorization for use and disclosure of protected health information.
  10. Agree to allow photographs of all selected lesions to be taken and/or send photos via text or email to the study team for assessment at 24 hours post treatment. Photos may be used as part of the study data and/or marketing package. (Photographs will be de-identified to those outside the research team. Effort will be made to ensure that no photos with identifiable features are obtained).

Exclusion Criteria:

  1. Are unable to cooperate with the requirements or visits of the study, as determined by the investigator.
  2. Have molluscum venereum (sexually transmitted molluscum).
  3. Have active molluscum eczema.
  4. Are systemically immunosuppressed or are receiving treatments such as chemotherapy or other non-topical immunosuppressive agents.
  5. Have had any previous treatment of molluscum in the past 14 days including the use of cantharidin, antivirals, retinoids, curettage or freezing of lesions. Additional treatments for molluscum should not be implemented during the course of the study.
  6. Have history of illness or any dermatologic disorder, which, in the opinion of the investigator will interfere with accurate counting of lesions or increase the risk of adverse events.
  7. History or presence of clinically significant medical, psychiatric, or emotional condition or abnormality that in the opinion of the investigator would compromise the safety of the subject or the quality of the data.
  8. Have a history or presence of hypersensitivity or an idiosyncratic reaction to the Study drug or related compounds, or drug product excipients.
  9. Have a condition or situation that may interfere significantly with the subject's participation in the study (e.g., patients who required hospitalization in the 2 months prior to screening for an acute or chronic condition including alcohol or drug abuse), at the discretion of the investigator.
  10. Have received another investigational product within 14 days prior to the first application of the Study drug.
  11. Have been treated within 14 days with a product that contains the active ingredient in VP-102 (topical or homeopathic preparations) for any reason prior to screening.
  12. Are sexually active or may become sexually active and are unwilling to practice responsible birth control methods. Females that have reached menarche, must have a negative urine pregnancy test at screening and each visit prior to treatment with study medication.
  13. Are pregnant or breastfeeding.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03186378


Contacts
Contact: Danielle Addison (919)-433-2751 danielle.addison@paidion.com
Contact: Olivia Pearce (919)-433-2747 Olivia.Pearce@paidion.com

Locations
United States, Nebraska
Midwest Children's Health Recruiting
Lincoln, Nebraska, United States, 68522
Contact: Julie Lyton, CCRC    402-327-6065    julie.layton@mchri.com   
Contact: Colleen Jarzynka    402-327-6066    collen.jarzynka@mchri.com   
Principal Investigator: Bradford A Brabec, MD         
Sponsors and Collaborators
Verrica Pharmaceuticals Inc.
Paidion Research, Inc
Database Integrations
Cato Research
Instat services
Investigators
Study Director: Matthew Davidson, PhD Verrica Pharmaceuticals Inc.
  More Information

Responsible Party: Verrica Pharmaceuticals Inc.
ClinicalTrials.gov Identifier: NCT03186378     History of Changes
Other Study ID Numbers: VP-102-103
First Submitted: June 12, 2017
First Posted: June 14, 2017
Last Update Posted: June 15, 2017
Last Verified: June 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: Yes
Device Product Not Approved or Cleared by U.S. FDA: Yes
Pediatric Postmarket Surveillance of a Device Product: No
Product Manufactured in and Exported from the U.S.: Yes

Additional relevant MeSH terms:
Molluscum Contagiosum
Poxviridae Infections
DNA Virus Infections
Virus Diseases
Skin Diseases, Viral
Skin Diseases, Infectious
Skin Diseases