Our team of medical professionals is evaluating an oral investigational drug to see if it reduces the signs and symptoms of Crohn’s disease by lowering the immune response that causes inflammation in the digestive system.
Complete our brief prescreening form to see if you may qualify or learn more below.See if you may qualify for the study
The DIVERSITY1 study is evaluating an oral investigational drug for people with moderate to severe Crohn’s disease. The investigational drug is taken as a tablet once a day. This clinical research study will help determine if the investigational drug improves the signs and symptoms of Crohn’s disease.
Participants who complete DIVERSITY1 may have the opportunity to enroll in a long-term extension study in which they will continue to receive the investigational study drug they have been assigned. More information about DIVERSITY1 can also be found at clinicaltrials.gov.See if you may qualify for the study
If you meet the criteria based on your responses to our prescreening form, you will be able to provide your contact information to a local doctor conducting the study. Their staff will answer any questions and will further determine if you may qualify. However, only investigational study drugs will be provided, other drugs you are currently taking for your Crohn’s disease may not be paid for by the study.
Crohn’s disease is a disorder of the immune system that causes the digestive system to become inflamed. People with Crohn's disease may experience diarrhoea, abdominal pain, or weight loss, among other symptoms. Crohn's disease is also linked to a higher risk of other intestinal complications.
Doctors use clinical studies to test safety and how well investigational drugs work for specific conditions. In a clinical study, participants may receive investigational drugs that have not yet been approved by the local regulatory agency. Researchers perform tests and assessments to find out how people respond to the investigational drug.
The DIVERSITY1 study is evaluating a once-daily oral investigational drug to see if it reduces the sign and symptoms of Crohn’s disease. People who participate in the DIVERSITY1 study may have access to investigational study drug and study-related care from a local study doctor.
Clinical research studies are conducted to determine if potential new drugs are safe and if they work. Clinical research studies are performed according to government regulations that help protect the safety and rights of the study participants.
A clinical investigator is a medical researcher in charge of conducting a clinical study and ensuring the well-being of study volunteers. The investigators conducting the DIVERSITY and SELECTION clinical studies are all qualified licensed physicians and medical specialists.
An investigational drug or research study drug is a drug that has not yet been approved by the local country regulatory agency for prescription by doctors.
Yes, participation in any clinical research study is completely voluntary. If you decide to stop participating at any time, your exit will not affect the medical care you would otherwise receive.
Informed consent is the process of learning the key facts and details about a clinical research study. This information will be provided to you before you decide to participate and as new information becomes available during your continued participation throughout the study. Once you have read the informed consent and understand the details, including the risks and any potential benefits, you can decide whether or not to sign the document. The informed consent process also includes opportunities for you to ask questions about the study. No study-related procedures will take place without a signed informed consent form.
Information about your personal health will be kept private and confidential in an encrypted database in France by the company hosting this website, Neonstone Ltd. With your permission, the information you provide via the prescreening form on this website about your medical history and health condition will be transferred to the study doctor’s office. A representative from the study doctor’s office will contact you to further determine your interest and eligibility. Your personal information will not be disclosed to anyone outside of this clinical research study group without your consent unless disclosure is required by law or regulations of the FDA, EMA, or similar local country regulatory agencies.
After answering the questions in the prescreening form, you will also have the option to sign up for future updates to be notified about other Crohn's disease and ulcerative colitis clinical studies. Respondents who do not qualify in the online prescreening form, or who are unable to locate a convenient site, will also be able to opt-in for updates which may affect their ability to participate. If you opt to receive these updates, you may receive emails from us in the future but will have the option to decline further communications at any time.
These clinical studies are being conducted to find out whether the investigational drug is effective in treating the signs and symptoms of Crohn’s disease and ulcerative colitis.
Your answers to the questions in the online prescreening form will determine if you meet certain key criteria that are required to participate in the DIVERSITY1 or SELECTION1 studies. If you meet these criteria, you can provide your contact information to the participating doctor’s office of your choice via our website. Their staff will then answer any questions you may have and will discuss the next steps to further determine whether you meet all of the criteria for participation. Not all people who complete the online prescreening form will be able to participate in one of the studies.
If you meet the criteria in the prescreening form, the staff at the doctor’s office will ask you to review and sign an informed consent form that explains more about the study. Then the staff at the doctor’s office will ask more questions and run some medical tests to see if you meet all eligibility criteria to participate in the clinical research study.
If you qualify for DIVERSITY1 or SELECTION1, you will come to the study doctor’s office for periodic visits for study exams to evaluate your general health and to discuss your Crohn’s disease or ulcerative colitis.
Feel free to discuss your study-related medical care with the study doctor or staff at any time during the course of the research study. It is important to take all investigational study drugs as prescribed. You will answer questions regarding how you feel during your participation and whether the investigational study drugs have been taken at the appropriate times. Participants are encouraged to discuss study participation with their general practitioner.
The studies each consist of 14-21 visits. The visits are 1-8 weeks apart, over a period of approximately 58 weeks (about one year).
Approximately 1,320 people worldwide will be enrolled in the DIVERSITY1 study, and approximately 1,300 people will be enrolled in SELECTION1 study. These studies are looking for people who have moderate to severe active Crohn's disease or ulcerative colitis
If you participate, all study-related doctors’ visits, monitoring of your condition and the investigational study medications will be provided to you. Other drugs you may be taking for your Crohn’s disease or ulcerative colitis may not be paid for by the study. The study staff at the participating site will be able to answer any questions you may have.
Participants are encouraged to discuss study participation with their general practitioner.
The choice to participate in this study is entirely yours. Your primary care doctor does not have to give his or her permission or a referral for you to participate in this study. However, you should tell your primary care physician about your participation and keep him or her informed about the study. You should also keep the study doctor informed if your primary care physician changes your Crohn's disease or ulcerative colitis treatment or if there are other changes to your health during the study.
A long-term extension study is a clinical study that allows participants to continue on investigational study drug after they have finished their participation in the original study. After completion of DIVERSITY1 or SELECTION1, participants may have the opportunity to enroll in a long-term extension study of the investigational drug in Crohn’s disease or UC.
A placebo does not contain any active ingredients and looks the same as the investigational study drug. The use of a placebo is important in clinical research studies because it allows researchers to determine how well the active investigational study drug may be working.
Some people who participate in these studies will receive active investigational drug and some will receive placebo. Neither you nor the study doctor will be able to choose or know which study group you are in. However, the study doctor can find out if there is an emergency or if it is necessary to know for your health.
You could experience side effects associated with the investigational study drug. The study staff will discuss the known risks in detail with you before you decide to participate.
After a clinical study is complete, all of the information is collected and analysed to help determine the investigational drug’s safety and efficacy. Please consult with your study doctor or regular healthcare provider to determine your treatment options after you have completed the study
The DIVERSITY and SELECTION studies are being conducted by trained, qualified, and licensed medical doctors worldwide.