Prism Clinical Research

University Enterprise Laboratories is currently undergoing construction on the south side of the building. 

The south entrance will be closed starting Wednesday, July 18th2018 until further notice. 

FOR SCREENINGS: Please enter through the East entrance (closest side to Hwy 280). In order to get inside, please pick up the phone in the weather proof box. This will ring to the nurses station and a staff member will be able to let you in. 

Please tell them you are here for a screening appointment (if you know the study number even better!). 

If you pick up the phone and it doesn't have a dial tone, remain on the line until someone answers (it will still ring in the nurses station). 

If no one answers the phone please knock twice and then try calling again.

Thank you for your patience during the construction. 

Prism Staff 

Get started on the volunteer process by registering your basic information with our database. This information is provided to help us determine your eligibility for current and future studies.

If you have registered with Prism in the past, please call Dayna 651-724-5047 to update your profile or learn about available studies. 

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

 Unfortunately at this time, Prism can not allow volunteers who live over 200 miles away to participate in research studies. If you live out of state or over 200 miles away please call Geoff at 651-641-2911 with questions. 

We will not share or sell this info with any third party.

STOOL SAMPLE STUDY

CLINICAL RESEARCH STUDY: 1808

PRISM CLINICAL RESEARCH

PURPOSE:

• To evaluate gut microbiota in volunteers with a heart condition

GENERAL STUDY REQUIREMENTS:

•  Healthy Men and Women between 18 and 79 years of age and a BMI
• between 17.0 to 39.9 kg/m2.
• Medical conditions must be stable in the opinion of the study doctor.
• History of Cardiac event, intervention, evaluation or stress test

STUDY DURATION:

• There are no in Clinic Stays for this study.
• Return Clinic Visits: There may be up to 3 return clinic visits, including
• screening, if a stool sample cannot be provided by the volunteer on the day
• of their screening.
• Total study duration is approximately –3 - 28 days (including screening).

METHOD OF ADMINISTRATION:

• This is a sample collection study; no study drug will be administered.

STUDY COMPENSATION:

• Compensation for Study Participation Time Up To: $285.00

RECRUITMENT CONTACT:

Dayna 651-724-5047 or daynas@prismresearchinc.com

You can WIN TICKETS VIA Prism's Facebook page!

Have you LIKED Prism Clinical Research on Facebook?

Have you TAGGED Prism Clinical Research on Twitter?

Have you FOLLOWED Prism Clinical Research on Instagram?

Use the link below:↓

https://www.facebook.com/PrismResearch/

Simply help us get the word out about Prism Clinical Research and we’ll give you $100 for every friend you refer that completes a study.

It’s that easy! Make money with each referral, and there’s no limit to how many friends you can refer!

Rules:

• Subject must qualify for a study.
• Subject may not be referred more than one time.
• Subjects eligible for Referral: (1) Must not be in Prism Clinical Research database; (2) Must not have participated in any prior study at Prism.
• In the event that a subject is referred by multiple people, the first person who referred will receive payment.
• Eligibility will be determined by Prism. Prism reserves the right to revise or eliminate this program at any time without notice.

Prism Research has upcoming studies for individuals who have been diagnosed with Celiac Disease.  These FDA approved studies will help determine how an investigational drug being developed for Celiac Disease is broken down and removed from the body in volunteers diagnosed with Celiac Disease.

If you or someone you know has been diagnosed with Celiac Disease and are interested in being considered for these studies, please contact Dayna at 651-724-5047 or register with our database and we will call you. Participants who qualify will receive a no cost health evaluation in addition to financial compensation for study participation time.

Please contact Dayna at 651-724-5047 or daynas@prismresearchinc.com for more information on these upcoming studies for individuals diagnosed with Celiac Disease. 

Study 1823

Cour Pharmeceuticals New Drug August 21, 2017

COUR PHARMACEUTICALS Recieves FDA fast track designation for TIMP-GLIA January 10, 2018

Dayna: 651-724-5047

Prism Research has upcoming studies for individuals diagnosed with liver impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of liver impairment when compared to volunteers with normal liver function.

 If you or someone you know has been diagnosed with liver impairment and are interested in being considered for these studies, please contact Dayna at 651-724-5047 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

Please contact Dayna at 651-724-5047 or daynas@prismresearchinc.com

Current Studies: 1813 & 1817

Prism Research has upcoming studies for individuals diagnosed with kidney impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of kidney impairment when compared to volunteers with normal kidney function.

 If you or someone you know has been diagnosed with kidney impairment and are interested in being considered for these studies, please contact Lindsay at 651-368-3360 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

Please contact Lindsay at 651-368-3360 or lindsayd@prismresearchinc.com

Renal Impairment Study

Clinical RESEARCH study: 1812

PRISM Clinical RESEARCH

Purpose:

•  A research study to evaluate the safety and tolerability of an investigational drug in individuals with renal impairment compared with individuals without renal impairment.

GENERAL STUDY REQUIREMENTS:

•  Men and Women Who are not able to become pregnant, between the ages of 18 to 75 with a BMI between 17.5 and 36 kg/m2.
•  Medical conditions and medications must be stable in the opinion of the study doctor.

STUDY DURATION:

•  In Clinic Stay: 6 nights/7 days.
•  Clinic Visits: up to 3 including screening and possible Follow-up visit.
•  Total study duration is approximately 6 weeks (including a 14-day screening period).

METHOD OF ADMINISTRATION:

•  Oral Administration

STUDY COMPENSATION:

•  Compensation for Study Participation Time Up To: $2,385.00

RECRUITMENT CONTACT:

•  Lindsay 651-368-3360 or lindsayd@prismresearchinc.com

Abnormal Liver Function Study

CLINICAL RESEARCH STUDY: 1813

PRISM CLINICAL RESEARCH

PURPOSE:

To determine how the investigational drug is absorbed, broken down, and removed from the body in volunteers with abnormal liver function compared to volunteers with normal liver function.

GENERAL STUDY REQUIREMENTS:

• Men and Women Between the ages of 18 and 70 years old.
• Abnormal liver function volunteers: must have mild/moderate abnormal liver function due to diagnosed liver disease.
• Healthy volunteers: must be healthy; not being evaluated or treated for any medical conditions.

STUDY DURATION:

• 1 In-Clinic Stay: Lasting 4 nights/ 5 days
• Up to 2 clinic visits for Screening
• 1 Follow Up Phone Call or clinic visit
• Total Study Duration is Approximately 64 days, including screening

METHOD OF ADMINISTRATION:

• Oral Administration

STUDY COMPENSATION:

• Compensation for Study Participation may be provided for time and travel up to $1785.00

RECRUITMENT CONTACT:

• Dayna 651-724-5047 or daynas@prismresearchinc.com

LIVER IMPAIRMENT STUDY

CLINICAL RESEARCH STUDY: 1817

PRISM CLINICAL RESEARCH

PURPOSE:

• To determine how the investigational drug is absorbed, broken down, and removed from the body in volunteers with abnormal liver function compared to volunteers with normal liver function.

GENERAL STUDY REQUIREMENTS:

• Men and women between the ages of 18 and 80 years old.
• Liver Impairment volunteers: must have mild/moderate/severe liver impairment due to diagnosed liver disease.
• Healthy volunteers: must be healthy; not being evaluated or treated for any medical conditions.

STUDY DURATION:

• 1 In-Clinic Stay: Lasting 8 nights/ 9 days
• Clinic Visits: 1(screening)
• Total Study Duration is Approximately 39 days, including screening

METHOD OF ADMINISTRATION:

• Oral Administration

STUDY COMPENSATION:

• Compensation for Study Participation may be provided for time and travel up to $2620.00

RECRUITMENT CONTACT:

• Jenna 651-724-0500 or jennal@prismresearchinc.com

HEALTHY FEMALE AND MALE PARTICIPANTS

CLINICAL RESEARCH STUDY: 1821

PRISM RESEARCH

PURPOSE:

 To evaluate the safety, tolerability, and pharmacokinetics of an investigational drug being developed for the treatment of certain types of cancer.

GENERAL STUDY REQUIREMENTS:

• Men and women who are 18 – 55 with a BMI between 18.5 to 29.9
• Must be non-smoker
• 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

STUDY DURATION:

• In Clinic Stay: 9 overnight stays consisting of 3 nights/4 days each period (total of 3 periods)
• Return Clinic Visits: 7 (including screen)
• Total study duration is approximately 50 days

METHOD OF ADMINISTRATION:

• Oral Administration

STUDY COMPENSATION:

• Compensation for Study Participation Time Up To: $3219.00

RECRUITMENT CONTACT:

• Jenna 651-725-0500 or jennal@prismresearchinc.com

Renal Impairment Study

Clinical RESEARCH study: 1822

PRISM CLINICAL RESEARCH

 Purpose:

•  To assess the pharmacokinetics and to evaluate the safety of an investigational drug in individuals with severe renal impairment versus individuals with normal renal function.

GENERAL STUDY REQUIREMENTS:

•  Men and Women, between the ages of 18 and 80
•  Medical conditions and medications must be stable in the opinion of the study doctor.
•  Volunteers must agree to use contraception, if applicable

STUDY DURATION:

• In Clinic Stay: 1 in clinic stay of approximately 72 hours, including 24 hours infusion of study drug.
•  Clinic Visits: 3, including screening visit, visit for PK sample collections and follow up visit.
•  Total study duration is approximately 38 days (including a 21-day screening period).

METHOD OF ADMINISTRATION:

•  Intravenous

REIMBURSEMENT:

•  Reimbursement  for reasonable expenses in connection with your Study Participation Up To $1240.

RECRUITMENT CONTACT:

•  Lindsay 651-368-3360 or lindsayd@prismresearchinc.com

Celiac Disease Study

CLINICAL RESEARCH STUDY: 1823

PRISM CLINICAL RESEARCH

Purpose:

• To evaluate an investigational drug being developed for the treatment of Celiac Disease.

GENERAL STUDY REQUIREMENTS:

• Men and Women who are willing to use an acceptable form of birth control, between the ages of 18 to 70 years old.
• Diagnosed by biopsy with Celiac Disease
• Gluten Free Diet for at least 6 months

STUDY DURATION:

• Clinic Visits: up to 10 including screening
• Total study duration is approximately 3 - 4 months

METHOD OF ADMINISTRATION:

•  Intravenous Administration

STUDY COMPENSATION:

• Compensation for Study Participation Time Up To: $2300

RECRUITMENT CONTACT:

• Dayna 651-724-5047 or daynas@prismresearchinc.com

Renal Impairment Study

Clinical RESEARCH study: 1900

PRISM RESEARCH

Purpose:

• To evaluate the safety and tolerability of an investigational drug in individuals with type 1 or type 2 diabetes who have been diagnosed with moderate to severe renal impairment.

GENERAL STUDY REQUIREMENTS:

• Men and women who are 18 years or older with a BMI between 18 and 45
• Medical conditions and medications must be stable in the opinion of the study doctor.

STUDY DURATION:

• In Clinic Stay: 2 nights/ 3 days
• Return Clinic Visits: 6 including screening
• Total study duration is approximately 33 days

METHOD OF ADMINISTRATION:

• A single subcutaneous injection

STUDY COMPENSATION:

• Compensation for study participation time up to $1470.00

RECRUITMENT CONTACT:

• Jenna 651-725-0500 or jennal@prismresearchinc.com

 Prism has a variety of upcoming studies to participate in: 

• Studies for healthy males and females 
• Liver Impairment 
• Multiple Sclerosis
• Kidney Impairment 
• Diabetes

To be put on the call list and receive more information, when available, please contact Dayna at daynas@prismresearchinc.com or Lindsay at lindsayd@prismresearchinc.com.