With your help, we can help advance medical knowledge and improve the health and well-being of countless others.
Our goal is to assist the pharmaceutical and medical device industries develop new and effective products to treat a multitude of medical conditions and illnesses. We perform this important work through the administration of clinical trials.
Please consider joining us in this effort. Our experienced and professional clinical research staff are highly qualified and fully committed to engaging you and your primary care physician as informed partners in everything we do.
Available Studies
See if you pre-qualify for any of the research studies we are now conducting in your area by following one of the links below.
Investigational COVID-19 Oral Tablet Vaccine Trial
Qualified participants must:
• have received 2 or more mRNA shots against COVID-19, such as Moderna or Pfizer.
• have had their last COVID-19 shot at least 6 months before taking part in the study
• meet other study criteria
Qualified participants will receive all study-related care at no cost. Reimbursement is available up to $770.00 for study-related time and travel.
By participating in this investigational study, you’ll have the opportunity to contribute to the ongoing efforts in the fight against COVID-19. Your involvement could potentially help advance the development of an oral tablet vaccine, which would be a significant step forward in combatting this global health crisis.
If you are interested in learning more, call AMR today at 888-259-1231 or fill out the form below and a member of our recruitment team will contact you to get started.
AMR Lexington is accepting volunteers for an investigational Asthma clinical research study.
Qualified participants must:
· be 18 to 55 years of age
· have moderate to severe uncontrolled asthma
· have documented diagnosis of asthma 12 months prior to screening visit
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related medical exams
· lab tests
· investigational medication or placebo
· study-related care overseen by a licensed Physician
Compensation up to $1,240.00 is available for time and travel. Insurance is not required.
Cardiovascular disease is risky business! That’s why AMR Lexington is conducting a clinical trial of an investigational medication to potentially reduce major adverse cardiovascular events in those with a previous history of adverse cardiovascular events and in those who are at high cardiovascular risk.
Qualified participants must:
· be ages 18 and older with a history of a major cardiovascular event Or
· be ages 50 and older who are at high risk for having their first major cardiovascular event
· meet other study criteria
Qualified participants will receive:
· all study-related care and the investigational medication or placebo at no cost
· compensation up to $2,550.00 for time and travel
Learn more by calling AMR Lexington at 888-259-1231 today!
AMR is currently accepting volunteers to participate in a high cholesterol clinical research study. Qualified participants are those ages 18 and older who meet other study criteria. Qualified participants will receive all study-related care and the investigational treatment or placebo at no cost. Compensation may be available up to $1,350.00 for study-related time and travel.
Diabetic Peripheral Neuropathic Pain: the most common type of diabetic neuropathy that affects the feet and legs first. It significantly impacts the quality of life in walking ability, sleep, work, and general activity. Currently, there are only four medications approved by the FDA for DPNP and clinical guidelines recommend pain relief through antidepressants, opioids, and topical medications. AMR Lexington is evaluating an investigational medication in adult participants with Diabetic Peripheral Neuropathic Pain to potentially lessen pain intensity.
Qualified participants must:
· be 18 and older
· have Type 1 Diabetes or Type 2 Diabetes diagnosed at least six months prior
· be on a stable diabetes treatment
· be willing to have a metformin dose modification
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related care and health monitoring
· the investigational medication or placebo
Compensation is available up to $1,533.00 for time and travel. To learn more, call AMR Lexington at 888-259-1231 today.
Join a clinical study of an investigational RSV/hMPV mRNA vaccine. AMR is conducting an investigational Respiratory Syncytial Virus and human MetaPneumo Virus mRNA vaccine clinical trial and is seeking healthy seniors to participate.
Qualified participants must:
· be 60 and older
· be considered healthy
· meet other study criteria
Receive study-related care and the investigational vaccine or placebo at no cost.
Compensation is available up to $2,010.00 for time and travel. Learn more by calling AMR at 888-259-1231 today.
AMR Lexington is conducting a study to test an investigational weight loss medication for overweight or obese Type 2 Diabetics.
Qualified participants must:
· be ages 18 and older
· be on stable treatment or diet and exercise for Type 2 Diabetes
· have a BMI of 27 or greater
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related care
· the investigational study drug or placebo
Compensation for time and travel may be provided. Learn more today! Call AMR Lexington at 888-259-1231.
AMR Lexington is currently seeking healthy volunteers to participate in a clinical research study of an investigational medication to prevent Botulism.
Qualified participants must:
• be a healthy adult 18 to 65 years of age
• meet other study criteria
Qualified participants will receive at no cost:
• all study-related medical exams
• lab tests
• injection of the investigational medication or placebo
Reimbursement for time and study-related travel is available up to $2,450.00. Insurance is not required.
To see if you qualify, call:
AMR Lexington at 888-259-1231
AMR Lexington is seeking healthy adults ages 18 and older for an investigational bird flu vaccine clinical study. Qualified participants will receive all study-related care and the investigational vaccine at no cost. Reimbursement for study-related time and travel is available up to $1,050.00.
Qualified participants must:
• be adults ages 18 and older
• be considered healthy
• meet other study eligibility criteria
To learn more, call AMR Lexington today at 888-259-1231.
AMR would like to invite you to participate in an Influenza Vaccine clinical research study happening now.
Qualified participants must:
• be 50 to 64 years of age
• meet additional study criteria
Receive all study-related care and the study vaccine at no cost. Compensation may be available for time and travel.
To learn more, call AMR at 888-259-1231.
Attention Smokers ages 21 to 60: AMR Lexington is conducting a clinical research study for nicotine oral products.
Participants will be daily cigarette smokers, have the availability to stay in-clinic for 10 days and 9 nights, and meet all study criteria. Compensation up to $4,400 may be available for your time and insurance is not required.
To find out how you can get involved call us today at 888-259-1231 or fill out the form below and a member of our recruitment team will contact you to get started.
Have you considered volunteering for a clinical research study for weight loss? If yes, Alliance for Multispecialty Research is enrolling adults 18 years of age or older who are considered obese or overweight for a weight reduction trial.
Volunteers will complete 14 visits at the study center over 54 weeks and compensation up to $2,100 will be available for time and travel.
To find out how you can get involved call us today at 888-259-1231 or fill out the form below and a member of our recruitment team will contact you to get started.
Did you receive an AREXVY vaccine 1.5 years ago? If yes, participate in a RSV booster vaccine study with AMR Lexington today! Study compensation for your time and travel up to $795 is available for qualified participants. Qualified participants must be 60 to 85, have received no more than one dose of AREXVY at least 1.5 years before study enrollment, and meet other study criteria
If you are interested in learning more, call AMR today at 888-259-1231 or fill out the form below and a member of our recruitment team will contact you to get started.
AMR Lexington is currently enrolling healthy volunteers ages 50 and older in an investigational Shingles vaccine study. Participants must have no history of Shingles, have never received a Shingles vaccine, and meet other study criteria. Receive all study-related care and the investigational vaccine at no cost. Compensation for study-related time and travel is available up to $2,060.00.
If you are interested in learning more, call AMR today at 888-259-1231 or fill out the form below and a member of our recruitment team will contact you to get started.
AMR Lexington is currently enrolling participants in an Osteoarthritis (OA) of the Knee clinical research trial for those 50 to 80 years old. Qualified participants must have a confirmed diagnosis of OA of the Knee, confirmed by x-ray, and meet other study criteria. Qualified participants will receive all study-related care at no cost. Compensation is available up to $950.00 for study-related time and travel.
If you are interested in learning more, call AMR today at 888-259-1231 or fill out the form below and a member of our recruitment team will contact you to get started.
AMR-Clinical Lexington is seeking participants 18 or older who are obese or overweight for a weight loss study. Qualified participants must have a BMI of 30 or higher or have a BMI 27 or higher with one medical condition such as high blood pressure, high cholesterol, sleep apnea, or heart disease, must not have Type 2 diabetes and meet other study criteria. Qualified participants will receive all study-related care at no cost. Compensation is available up to $7,700.00 for study-related time and travel.
If you are interested in learning more, call AMR-Clinical today at 888-259-1231 or fill out the form be-low and a member of our recruitment team will contact you to get started.
AMR Lexington is conducting an investigational Type 2 Diabetes trial for participants ages 18 to 75. Qualified participants must have Type 2 Diabetes, a BMI of 27 or greater, be on a stable GLP-1 dose for at least 6 months, and meet other study criteria. Qualified participants will receive all study-related care at no cost. Reimbursement is available up to $2,250.00 for study-related time and travel.
If you are interested in learning more, call AMR today at 702-529-0153 or fill out the form below and a member of our recruitment team will contact you to get started.
Frequently Asked Questions
In Phase I trials, researchers test an experimental drug or treatment in a small group of people (20-80) for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
In Phase II trials, the experimental study drug or treatment is given to a larger group of people (100-300) to see if it is effective and to further evaluate its safety.
In Phase III trials, the experimental study drug or treatment is given to large groups of people (1,000-3,000) to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the experimental drug or treatment to be used safely.
A protocol is a study plan on which all clinical trials are based. The plan is carefully designed to safeguard the health of the participants as well as answer specific research questions. A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study. While in a clinical trial, participants following a protocol are seen regularly by the research staff to monitor their health and to determine the safety and effectiveness of their treatment.
Clinical trials that are well-designed and well-executed are the best approach for eligible participants to:
Play an active role in their own health care.
Gain access to new research treatments before they are widely available.
Obtain expert medical care at leading healthcare facilities during the trial.
Help others by contributing to medical research.
Risks
There are risks to clinical trials.
There may be unpleasant, serious or even life-threatening side effects to experimental treatment.
The experimental treatment may not be effective for the participant.
The protocol may require more of their time and attention than would a non-protocol treatment, including trips to the study site, more treatments, hospital stays or complex dosage requirements.
Some clinical trials involve more tests and doctor visits than the participant would normally have for an illness or condition. For all types of trials, the participant works with a research team. Clinical trial participation is most successful when the protocol is carefully followed and there is frequent contact with the research staff.
All clinical trials have guidelines about who can participate. Using inclusion/exclusion criteria is an important principle of medical research that helps to produce reliable results. The factors that allow someone to participate in a clinical trial are called “inclusion criteria” and those that disallow someone from participating are called “exclusion criteria”. These criteria are based on such factors as age, gender, the type and stage of a disease, previous treatment history, and other medical conditions. Before joining a clinical trial, a participant must qualify for the study. Some research studies seek participants with illnesses or conditions to be studied in the clinical trial, while others need healthy participants. It is important to note that inclusion and exclusion criteria are not used to reject people personally. Instead, the criteria are used to identify appropriate participants and keep them safe. The criteria help ensure that researchers will be able to answer the questions they plan to study
Participants in clinical trials can play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research.
Although there are many definitions of clinical trials, they are generally considered to be biomedical or health-related research studies in human beings that follow a predefined protocol. ClinicalTrials.gov includes both interventional and observational types of studies. Interventional studies are those in which the research subjects are assigned by the investigator to a treatment or other intervention, and their outcomes are measured. Observational studies are those in which individuals are observed and their outcomes are measured by the investigators.
Volunteer Form
By volunteering for clinical studies, you authorize AMR to store your personal information on file. In accordance with HIPAA regulations, AMR will never share your information with anyone.
Respiratory Syncytial Virus
It is estimated that more than 177,000 older adults are hospitalized and 14,000 of them die in the US due to RSV infections per year. In 2018, more elder Americans died from RSV infection than the common flu.
To learn more, call our enrollment line:
Refer-A-Friend
Earn extra cash* by recommending a friend to us and receive up to $100 for each friend you refer!
Read Important Instructions
* Some restrictions apply. Not all studies are eligible for the Refer-A-Friend program. Ask an AMR representative for details.
Refer-A-Friend
Step 1
Fill out the Refer-A-Friend form. You can download the form here or pick one up at one of our offices. The referrer (you) must fill out the form.
Step 2
Your friend or family member brings the completed referral form to CRC on their first visit to our office and gives it to a staff member upon checking in.
Step 3
If your referral qualifies for and completes all visits for the study, you (the referrer) will earn $100 upon study completion.
