Research Center

Clinical Research Group of Montana, PLLC has conducted drug trials for eight years, resulting in several publications and research grants, and the FDA approval of several new medications. Prior to moving to Montana, Dr Wanderer headed a similar drug trial research center in Denver, Colorado for 25 years. We are proud of our combined 33 years of experience in the research of asthma and allergic diseases with supervision of over 150 clinical drug trials. Dr Wanderer is certified as a physician investigator (CPI), based on his years of clinical drug trial experience and having passed a written examination in drug research. He is Board Certified in Pediatrics and in Allergy and Immunology. Dr. DiCello also has experience in drug trials from when he was practicing in South Burlington, VT. He is Board Certified in Internal Medicine and in Allergy and Immunology.

Research Studies

We are always looking for children and adults who are interested in our research program. Participating in our research studies is an excellent way to learn more about controlling your allergy and/or asthma symptoms. Studies at the Clinical Research Group of Montana have contributed to the approval of medications for the treatment of: No insurance is necessary and the research studies are free of charge. During participation, qualified individuals are compensated for their time and frequently receive free medical examinations, health laboratory tests and medications related to the research study.

Research study appointments can sometimes be scheduled before work or school, as early as 7 a.m.

Clinical Trials

A Clinical Trial is a study that is used to gather information about new medicines. Information obtained during these trials helps pharmaceutical researchers develop new and better medicines to treat all diseases. Most medicines prescribed today have been through numerous Clinical Trials before becoming available to the public. Patient safety is the utmost concern of the FDA, the pharmaceutical companies, and our research site.

Every precaution is taken to make certain the study participant understands and agrees to the study. Before participating in a study, volunteers must sign an Informed Consent form that gives detailed information regarding the study, medications, and procedures that will take place. Experienced investigators (clinical research physicians) and nurses (clinical research coordinators) closely monitor the participant during the course of the study.

All research studies must be reviewed by a committee called an Institutional Review Board (IRB). This committee consists of medical professionals and specialists in ethics. The IRB and our research center always have the study participant's best interests in mind, and will address any questions or concerns that the participant may have.
To learn more, please call (406) 585-2444. You can also stop by our research center at 2015 Charlotte Street, Suite 1, Bozeman, MT 59718 Map It

Why should I volunteer for a clinical trial?

By participating in a clinical trial, you are helping yourself and others like you to live healthier lives. Without volunteers, there would be no new drugs to fight diseases and ailments. Your volunteer efforts will contribute to the advancement of medical care. You may have the opportunity to receive a new medication to treat your condition. You also have the opportunity to learn more about your condition or disease, and about the latest research and treatments.

If you qualify as a volunteer, you receive all medical visits related to the study free of charge. This includes physical examinations, study medications, and laboratory tests. Compensation for your time and travel is also available.