Design of Study: All study participants receive Zyprexa. In addition to Zyprexa, half of the participants also receive Samidorphan and the other half receive a placebo instead of Samidorphan. You will be monitored for general safety, control of schizophrenia, safety, and weight.

Length of Study: Twenty (20) visits over 30 weeks.

Qualified Study Participants Will Receive:

• Study-related care and office visits at no cost
• Investigational study medication at no cost
• $75 compensation per visit

Am I Eligible for the Study?

• Aged 18 - 55 years old
• Diagnosed with schizophrenia
• Medically stable with a stable living residence

Why Should You Participate? Clinical trials are how all new medicines are tested. These trials can also look at other aspects of care, such as improving the quality of life for people with chronic illnesses. You may also help others by advancing science.

Interested in Participating? If you are interested in joining this study, please fill out the form below to provide your contact information, or call our office at (773) 989-8313 x 2 and leave a message on our screening line. A member of our staff will call you back within 24 hours and will conduct a short phone screen to determine if you should visit our office for further evaluation.

Studies Form

First Name *

Last Name *

Email Address *

Phone Number *

Study Name *

Please write or copy and paste the study name listed above here.

Message

Please let us know any additional information here.

Design of Study: This is an outpatient study. Participants will receive either Zyprexa or Risperdal for the first part of the study. If they fully respond to one of these medications, their participation ends and they do not receive the study drug. If they do not fully respond they are assigned to take the new study drug or to stay on the Zyprexa or Risperdal. At the study’s completion, participants have the option to take the study medication for one year.

Length of Study: Fourteen (14) visits over 22 weeks.

Qualified Study Participants Will Receive:

• Study-related care, inpatient care, and office visits at no cost
• Investigational study medication at no cost
• $75 compensation per visit

Am I Eligible for the Study?

• Aged 18 or over
• Diagnosed with Schizophrenia
• Have an identified caregiver or family member
• Medically stable with a stable living residence

Why Should You Participate? All new medicines are tested in clinical trials. You may also help others by advancing science, and you may gain access to a new treatment.

Interested in Participating? If you are interested in joining this study, please fill out the form below to provide your contact information, or call our office at (773) 989-8313 x 2 and leave a message on our screening line. A member of our staff will call you back within 24 hours and will conduct a short phone screen to determine if you should visit our office for further evaluation.

Studies Form

First Name *

Last Name *

Email Address *

Phone Number *

Study Name *

Please write or copy and paste the study name listed above here.

Message

Please let us know any additional information here.

Design of Study: This is an inpatient study. Participants are required to remain in the hospital for 3-4 weeks and must agree to stop current medications used to treat their Bipolar Disorder. Participants will receive Brexpiprazole or a placebo.

Length of Study: Approximately 8 weeks. (including a 3-4 week inpatient hospital stay).

Qualified Study Participants Will Receive:

• Study-related care, inpatient care, and office visits at no cost
• Investigational study medication at no cost
• $75 compensation per visit

Am I Eligible for the Study?

• Aged 18 - 65 years old
• Diagnosed with Bipolar 1 and experiencing an acute manic episode
• History of at least one prior manic episode that required intervention or hospitalization
• Medically stable with a stable living residence

Why Should You Participate? All new medicines are tested in clinical trials. You may also help others by advancing science, and you may gain access to a new treatment.

Interested in Participating? If you are interested in joining this study, please fill out the form below to provide your contact information, or call our office at (773) 989-8313 x 2 and leave a message on our screening line. A member of our staff will call you back within 24 hours and will conduct a short phone screen to determine if you should visit our office for further evaluation.

Studies Form

First Name *

Last Name *

Email Address *

Phone Number *

Study Name *

Please write or copy and paste the study name listed above here.

Message

Please let us know any additional information here.

Design of Study: This is an outpatient study and all participants will receive either the study medication or a placebo. Participants on Depakote or Lithium may stay on these medications throughout the study.

Length of Study: Nine (9) visits over 10 weeks.

Qualified Study Participants Will Receive:

• Study-related care and office visits at no cost
• Medication at no cost
• $75 compensation per visit

Am I Eligible for the Study?

• Aged 18 - 65 years old
• Diagnosis of Bipolar Disorder
• Current depressive episode lasting from 2 weeks to 6 months
• Medically stable with a stable living residence

Why Should You Participate? Clinical trials are how all new medicines are tested. These trials can also look at other aspects of care, such as improving the quality of life for people with chronic illnesses. You may also help others by advancing science and may gain access to a new treatment.

Interested in Participating? If you are interested in joining this study, please fill out the form below to provide your contact information, or call our office at (773) 989-8313 x 2 and leave a message on our screening line. A member of our staff will call you back within 24 hours and will conduct a short phone screen to determine if you should visit our office for further evaluation.

Studies Form

First Name *

Last Name *

Email Address *

Phone Number *

Study Name *

Please write or copy and paste the study name listed above here.

Message

Please let us know any additional information here.

Design of Study: This is an outpatient study open to individuals with military-related PTSD. Subjects will receive either the study medication or a placebo (“sugar pill”). At the end of the study, all participants have the option to continue on the active study medication.

Length of Study: 12 Weeks; with an option to rollover into a treatment only study at the end.

Qualified Study Participants Will Receive:

• Study-related care and office visits at no cost
• Medication at no cost
• $75 compensation per visit

Am I Eligible for the Study?

• Aged 18 - 75 years old
• A diagnosis of military-related PTSD, and can show proof of service since 2001
• Willing and able to withdraw from prohibited medications for the duration of the study
• Medically stable with a stable living residence

Why Should You Participate? This study offers state-of-the-art care tailored to adults with military-related PTSD at no cost to the participant. You may also help others by advancing science.

Interested in Participating? If you are interested in joining this study, please fill out the form below to provide your contact information, or call our office at (773) 989-8313 x 2 and leave a message on our screening line. A member of our staff will call you back within 24 hours and will conduct a short phone screen to determine if you should visit our office for further evaluation.

Studies Form

First Name *

Last Name *

Email Address *

Phone Number *

Study Name *

Please write or copy and paste the study name listed above here.

Message

Please let us know any additional information here.

Design of Study: This is an outpatient study and all participants will be on commercially available branded medication for the study duration. Participants start on Invega pills and have a chance of receiving the injectable Invega Sustenna. They may be changed to other approved medications as clinically needed. In addition to assessing symptoms of psychosis, the study examines functional outcomes, such as the use of medical resources and involvement in school and work. All participants require an identified “informant,” such as a caregiver or family member, who can report on their well-being.

Length of Study: Approximately 50 visits over two years.

Qualified Study Participants Will Receive:

• Study-related care and office visits at no cost
• Medication at no cost
• Patient and “informant”will each receive $75 compensation per visit

Am I Eligible for the Study?

• Aged 18 - 35 years old
• First psychotic episode within two years of study entry
• Have an identified caregiver or family member
• Medically stable with a stable living residence

Why Should You Participate? This study offers state-of-the-art care tailored to young adults with a recent onset of symptoms. You may also help others by advancing science.

Interested in Participating? If you are interested in joining this study, please fill out the form below to provide your contact information, or call our office at (773) 989-8313 x 2 and leave a message on our screening line. A member of our staff will call you back within 24 hours and will conduct a short phone screen to determine if you should visit our office for further evaluation.

Studies Form

First Name *

Last Name *

Email Address *

Phone Number *

Study Name *

Please write or copy and paste the study name listed above here.

Message

Please let us know any additional information here.

Design of Study: This is a randomized, double-blind, placebo-controlled study.

Length of Study: The total study duration for a subject will be approximately one year with the possibility of continuing on the same medication in a follow-up open-label study.

Qualified Study Participants Will Receive:

• Study-related care and office visits at no cost
• Medication at no cost
• $75.00 per completed office visit; $30 per completed telephone visit

Am I Eligible for the Study?

• Aged 18 - 65 years old
• Diagnosed with schizophrenia
• Has been responsive to an antipsychotic treatment (other than clozapine) in the past year
• Willing to take “add-on” medication
• Medically stable with a stable living residence

Why Should You Participate?

• Receive the newest and latest treatments in psychiatry.
• Help yourself and others by contributing to medical research.
• Receive study-related care and medication at no cost to you or your insurance provider.
• Financial compensation for participation.
• Remember: every single medication that is currently used for psychiatric care was once studied as part of a clinical trial.

Interested in Participating? If you are interested in joining this study, please click on the “Sign Up” button below to provide your contact information, or call our office at (773) 989-8313 x 2 and leave a message on our screening line. A member of our staff will call you back conduct a short phone screen to determine if you should visit our office for further evaluation.

Studies Form
First Name *
Last Name *
Email Address *
Phone Number *
Study Name *
Please write or copy and paste the study name listed above here.
Message
Please let us know any additional information here.