MedPath

VPD-737 for Treatment of Chronic Pruritus

Phase 2
Completed
Conditions
Chronic Pruritus
Interventions
Drug: VPD-737
Drug: Placebo
Registration Number
NCT01951274
Lead Sponsor
Vyne Therapeutics Inc.
Brief Summary

A study of a several doses of a novel treatment for chronic itch compared to placebo for patients whose condition has not responded to other treatments

Detailed Description

The sensation of itch is transmitted to the brain through the nervous system Several chemicals are involved in transmitting this signal This trial of VPD 737 is intended to treat this condition by blocking one of the chemicals involved in the transmission of the itch signal This is an oral drug administered once daily It has been used in other trials and has shown to be safe at the doses used in this trial The trial will involve once daily pills for 6 weeks. Subject will be asked to fill out questionnaires both electronically and on paper during the study period Patients will also be monitored for safety and will have blood taken for testing and several points during the trial Overall participation will last about 12 weeks

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
257
Inclusion Criteria
  • Clinical diagnosis of chronic pruritus and unresponsive to current therapies
Read More
Exclusion Criteria
  • Have chronic liver or renal disease
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
0.25 mg VPD-737VPD-7370.25 mg of VPD-737 daily by mouth for 42 days
1 mg VPD-737VPD-7371 mg VPD-737 taken daily by mouth for 42 days
5 mg VPD-737VPD-7375 mg tablets of VPD-737 to be taken daily by mouth for 42 days
PlaceboPlaceboplacebo tablets to be taken daily by mouth for 42 days
Primary Outcome Measures
NameTimeMethod
Visual Analog Scale6 weeks
Secondary Outcome Measures
NameTimeMethod
Verbal Response Scale6 weeks

Trial Locations

Locations (25)

Stanford University, Medical Dermatology

🇺🇸

Redwood City, California, United States

Dermatology of Boca

🇺🇸

Boca Raton, Florida, United States

Skin Care Research

🇺🇸

Boca Raton, Florida, United States

Shideler Clinical Research Center

🇺🇸

Carmel, Indiana, United States

Grekin Skin Institue

🇺🇸

Warren, Michigan, United States

Comprehensive Clinical Research

🇺🇸

Berlin, New Jersey, United States

Suzanne Bruce and Associates, P.A.

🇺🇸

Houston, Texas, United States

Quality Clinical Research Inc.

🇺🇸

Omaha, Nebraska, United States

The Center for Clinical and Cosmetic Research

🇺🇸

Aventura, Florida, United States

Temple University

🇺🇸

Philadelphia, Pennsylvania, United States

Dermatology Clinical Research Center of San Antonio

🇺🇸

San Antonio, Texas, United States

Dermatology Consulting Services

🇺🇸

High Point, North Carolina, United States

Advanced Medical Research, Inc.

🇺🇸

Atlanta, Georgia, United States

The Indiana Clinical Trials Center, PC

🇺🇸

Plainfield, Indiana, United States

Minnesota Clinical Study Center

🇺🇸

Fridley, Minnesota, United States

Baker Allergy, Asthma and Dermatology Research Center, LLC

🇺🇸

Lake Oswego, Oregon, United States

Marycliff Allergy Specialist

🇺🇸

Spokane, Washington, United States

Pfugerville Dermatology

🇺🇸

Pflugerville, Texas, United States

Center for Dermatology Clinical Research, Inc.

🇺🇸

Fremont, California, United States

Torrance Clinical Research Institute Inc.

🇺🇸

Lomita, California, United States

UCSD Dermatology

🇺🇸

San Diego, California, United States

Skin Search of Rochester, Inc.

🇺🇸

Rochester, New York, United States

The Dermatology Group, P.C.

🇺🇸

Verona, New Jersey, United States

Olympian Clinical Research

🇺🇸

Tampa, Florida, United States

WestEnd Dermatology Associates

🇺🇸

Richmond, Virginia, United States

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