Research Studies

Current Clinical Trials:

Study: Injectable Treatment to Treat Keloids

Purpose: To assess the safety, tolerability, and efficacy of various doses of STP705 (10μg, 20μg, 30μg and 40μg) intradermal injection and placebo, when injected into the keloid excision site, to prevent the recurrence of keloids following their excision. The study treatments are administered once per week. There will be four (4) follow-up visits at one (1), three (3), six (6) and nine (9) months after your keloid surgery.

Qualifications:

• Male and Females, 18 – 60 years old
• Have at least one keloid scar present for at least one year on the upper body, arms, or legs

Duration: 54 weeks

Location: Hackensack, NJ

Compensation: Up to $1,100 if all study visits are completed

To participate Please click here.

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Study: Evaluation of the Mind.Px Patch on Response to Biologic Treatment for Patients with Plaque Psoriasis

Purpose: The purpose of this study is to evaluate the impact of Mind.Px on response to biologic treatment for patients suffering from plaque psoriasis, as judged by the mean change in the Psoriasis Area Severity index (PASI) score from baseline to end of Week 16 of the study.

Qualifications:

• Male and Females, 18 years or older
• Current diagnosis of Plaque Psoriasis

Duration: Up to 20 weeks

Location: Hackensack, NJ

Compensation: Up to $630 will be paid to the patient *once all visits are completed*

Interested in participating in our clinical research study? Please click here.

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Study: Evaluation of the risk of atrophic acne scar formation during treatment of acne vulgaris subjects with trifarotene 50 μg/g cream versus vehicle cream

Purpose: The purpose of this trial is to evaluate the effect of trifarotene 50 μg/g cream versus vehicle cream on the risk of formation of atrophic acne scars in facial acne subjects. This is a randomized, double-blind, vehicle-controlled clinical study using a split-face design for intra-individual comparison (right half-face versus left half-face).

Qualifications:

• Male and Females, 17 to 35 years old
• Clinical diagnosis of Acne Vulgaris on the face (minimum of 20 inflammatory lesions and minimum of 10 atrophic acne scars)
• Symmetrical number of lesions/scars on the whole face (i.e. no more than twice as many lesions/scars of each type on one half of the face than on the other half)

Duration: Up to 24 weeks

Location: Hackensack, NJ

Compensation: Up to $1,450

Interested in participating in our clinical research study? Please click here.

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Study: Efficacy and Safety study of RPT193 as Monotherapy in Adults with Moderate-to-Severe Atopic Dermatitis

Purpose: This study is being done to evaluate the safety and tolerability of RPT193 in subjects with moderate to severe atopic dermatitis, also known as eczema. Investigational product will be administered as monotherapy for AD in adult patients who have had an inadequate response to topical medications for AD (e.g., corticosteroids) or who are otherwise unable to take topical medications.

Qualifications:

• Male and Females, 18 to 75 years old
• Clinical diagnosis of Atopic Dermatitis
• Documented history of inadequate response to a ≥1 month treatment with topical medications

Duration: Up to 7 months

Location: Hackensack, NJ

Compensation: Up to $650

Interested in participating in our clinical research study? Please click here.

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Study: A Post Market Study of a 1726nm Laser System for the Treatment of Acne Vulgaris

Purpose: The purpose of this investigation is to evaluate the safety and efficacy of the Cutera® 1726 nm laser system for the treatment of moderate to severe acne. Subjects will receive 3 laser treatments at 4-week intervals. Follow-up visits will occur at approximately 7 days post each treatment (via phone) and at 12-, 26- and 52-weeks post third treatment.

Qualifications:

• Males and females, ages 16 to 60 years
• Fitzpatrick skin types I-VI with moderate or severe acne vulgaris

Duration: Approximately 17 months

Location: Hackensack, NJ

Compensation: Up to $275 will be paid to the patient *once all visits are completed*

Interested in participating in our clinical research study? Please click here.