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    Thanks for your interest, you'll find the intake form here

  • Study 1409: Healthy Male and Female (Not of Child Bearing Potential) Participants

    Research Purpose:  Study 1409 is designed to evaluate the dosing method of an investigational drug being developed for the treatment of psoriasis. The investigational drug will be given by subcutaneous (just below the skin) injection to healthy participants two times via syringe (once using 1 syringe and once using two syringes). The following will be evaluated:

    • How much of the investigational drug gets into the blood stream using both injection methods
    • How quickly the investigational drug enters and eliminates from the blood stream using both injection methods
    • The safety/tolerability of the investigational drug


    Minimum Screening Qualifications:


    Men are allowed to participate


    Women are allowed to participate only if they are postmenopausal or surgically sterilized by hysterectomy, tubal ligation, or bilateral oophorectomy


    18-55 years

    Body Mass Index (BMI)

    18 and 30


    110 and 242 pounds

    Tobacco/Nicotine Use

    No tobacco/nicotine use during In-house stays and outpatient visits.  Use of tobacco/nicotine products at all other times during the study is allowed.

    Drug Testing

    Must test negative for drugs of abuse. 

    Alcohol/Drug Abuse History

    No history of drug or alcohol abuse within 1 year of the screening appointment.

    Health History

    Must be healthy; not being evaluated or treated for any medical conditions unless otherwise approved on a case by case basis by the study doctor

    Restricted Medications

    No required regular use of any prescription medications, non-prescription medications, or vitamins not listed below

    Allowed Medications

    Hormone replacement therapy, thyroid medications, acetaminophen


    Study Time Commitment: For participants who qualify based on screening evaluation, study participation will last for approximately 9 weeks. 

    In-house Stays

    Participants will stay at Prism Clinical Research two times. 

    • In-house Stay 1:  2 ½ days (2 overnights)
    • In-house Stay 2: 1 ½ days (1 overnight).  This stay will take place approximately 1 month after the first In-house stay

    Office Visits

    Each In-house stay is followed by a set of brief office visits.

    • In-house Stay 1 is followed by 9 office visits over the course of 4 weeks
    • In-house Stay 2 is followed by 10 office visits over the course of 4 weeks and one follow up phone call. 

    Compensation: Up to $2500

Recruitment and Volunteer Demographics

Prism Clinical Research recognizes the need to continually grow our diverse volunteer database populations. Through a multi-faceted enrollment process that includes a dedicated recruitment department, collaborative physician partnerships, advertising and subject referral programs, Prism Clinical Research can deliver Phase I-II results in the following populations:

  • HIV

  • Hepatic

  • Renal (Pre-ESRD, ESRD)

  • Type 2 Diabetes

  • Obesity

  • Healthy Male/Female/Elderly

  • Gilbert’s subset

  • Rheumatoid Arthritis

  • Epilepsy

  • Multiple Sclerosis
  • GI (IBS & Crohn’s)

  • Celiac
  • COPD, Allergy and Asthma

  • High Cholesterol

  • Hypertensive

  • Alzheimer's Disease
  • Ophthalmology

  • Slow Metabolizers

  • Osteoporosis
  • Osteoarthritis
  • Lupus

Please provide us with your contact information (below) and will get back to you as soon as possible.

If you have a general question, check Volunteer FAQ for an answer. If you're unsure of who to contact, please visit the Contact Us page.