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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06103695
Other study ID # PTC10
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date February 27, 2023
Est. completion date October 18, 2023

Study information

Verified date October 2023
Source Psoriasis Treatment Center of Central New Jersey
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Open label study to assess 12 weeks of add-on VTAMA® (tapinarof) Cream, 1% QD in patients with ≥3% BSA who have received biologic therapy for at least 24 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 18, 2023
Est. primary completion date October 18, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Male or female adult = 18 years of age; 2. Diagnosis of chronic plaque-type 3. Patient with =3% BSA 4. Patient has been treated with biologic for a minimum of 24 weeks 5. Able and willing to give written informed consent prior to performance of any study-related procedures. Exclusion Criteria: 1. =3% BSA 2. Patient not receiving biologic agent, or receiving biologic agent <24weeks

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tapinarof
Add on Vtama (tapinarof) to biololgic therapy

Locations

Country Name City State
United States Schweiger Derm Group East Windsor New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Psoriasis Treatment Center of Central New Jersey

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Body surface area =1% Patients who achieve body surface area of =1% 12 weeks
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