Status:
UNKNOWN
Efficacy and Safety Study of Autonomic Nerve Modulation (ANM) in Subjects With Moderate Plaque Psoriasis
Lead Sponsor:
Thync Global, Inc.
Collaborating Sponsors:
ethica Clinical Research Inc.
Conditions:
Plaque Psoriasis
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This is a 16-week, prospective, multicenter, double-blind, controlled, randomized study assessing change in psoriasis severity and level of stress in patients with moderate psoriasis treated with ANM....
Eligibility Criteria
Inclusion
- Outpatient, male or female of any race, 18 years of age or older. This study has no pregnancy restrictions.
- BSA\* \<10% (excluding palms, soles, intertriginous and inverse areas).
- sPGA\* ≥3 (NOTE: sPGA score will be averaged across all lesions as opposed to grading target lesions).
- BSA x sPGA ≥12.
- Subject diagnosed with chronic plaque psoriasis at least 6 months prior to screening.
- Treatment-naïve of prohibited biological immunomodulating agents at the time of screening, or decided to stop treatment with the biologic before screening for the study.
- Be able to follow study instructions and likely to complete all required visits.
- Sign the IRB-approved ICF (which includes HIPAA).
Exclusion
- Non-plaque psoriasis (erythrodermic or pustular), guttate, inverse psoriatic arthritis, or drug-induced psoriasis.
- Subjects with plaque psoriasis on palms and soles at enrolment.
- Subjects with plaque psoriasis on the back of the neck that would interfere with device placement.
- Evidence of skin conditions other than psoriasis that would interfere with study-related evaluations of psoriasis.
- Other than psoriasis, history of any clinically significant (as determined by Investigator) or other major uncontrolled disease.
- Psoriasis flare or rebound within 4 weeks of Visit 1 or spontaneously improving or rapidly deteriorating plaque psoriasis during that same time period, as determined by investigator.
- Use of prohibited medications within the following washout periods:
- Biological immunomodulating agents within the prior 12 weeks: etanercept (Enbrel), adalimumab (Humira), infliximab (Remicade), certolizumab pegol (Cimzia), ixekizumab (Taltz)
- Biological immunomodulating agents within the prior 24 weeks: ustekinumab (Stelara), secukinumab (Cosentyx), guselkumba (Tremfaya)
- Oral drugs within the prior 4 weeks: apremilast, methotrexate, cyclosporine, corticosteroids
- Oral drugs within the prior 12 weeks: acitretin
- Photochemotherapy (PUVA) within the prior 4 weeks
- Phototherapy (UVA/UVB) within the prior 2 weeks
- Topical treatment likely to impact signs and symptoms of psoriasis (e.g., corticosteroids, vitamin D analogues, retinoids, calcineurin inhibitors, salicylic acid, lactic acid, tar, urea, etc.) within the prior 2 weeks
- Prolonged sun exposure or use of tanning booths or other source of UV radiation.
- Medical or psychiatric conditions that may increase the risk associated with study participation or may interfere with the interpretation of study results or compliance of the subject and, in the opinion of the PI, would make the subject inappropriate for entry into this study.
- Clinically significant alcohol or drug abuse, or history of poor cooperation or unreliability.
- Exposure to any other investigational drug/device within 30 days prior to study entry.
- Subjects with a pacemaker, or any type of metal implant in the neck (i.e., T5 and above).
Key Trial Info
Start Date :
October 2 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 30 2019
Estimated Enrollment :
110 Patients enrolled
Trial Details
Trial ID
NCT03817164
Start Date
October 2 2018
End Date
October 30 2019
Last Update
July 9 2019
Active Locations (1)
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1
Site 1
Fremont, California, United States, 94538