Frequently Asked Questions

Signs may include:¹

• Feeling nervous and irritable
• Slight tremor of the hands or fingers
• Heat sensitivity, with an increase in sweating or warm, moist skin
• Weight loss, despite wanting to eat more
• Having an enlarged thyroid gland
• Changes in menstrual cycles
• Having frequent bowel movements
• Fatigue
• Having fast or irregular heartbeat, called palpitations
• Not sleeping well

1. Source: https://www.mayoclinic.org/diseases-conditions/graves-disease/symptoms-causes/syc-20356240

While every study is different, currently enrolling local studies are looking for individuals ages 18 and older who:

• Have been diagnosed with Graves’ disease
• Are currently taking a steady, daily dose of medications to control it
• Have never had radioactive iodine therapy or surgery to remove their thyroid

Additional criteria apply. A study doctor will determine final eligibility based on full medical criteria.

The information gathered in clinical studies may help identify new treatment options in the future for people living with Graves’disease. Study participants are often connected to specialists who understand their situation and can help answer questions from patients or their loved ones. 

Participants in research studies should expect to experience a professional clinical environment, be treated with compassion and respect, and have access to top quality study-related care during the clinical trial.

Most clinical trials will involve a screening visit to confirm that a potential participant is, in fact, a match for that trial’s criteria. Once verified, an Informed Consent Form, which clearly provides the details and purpose of the trial to that individual and what it involves, is reviewed, with the participant to sign. 

Participants can then expect to attend scheduled appointments at a trial clinician’s site. They may also receive a trial treatment (also called an investigational product) or a control (also known as placebo, which contains no active treatment) and undergo additional  assessments  and follow-up monitoring. 

Throughout the trial, participants should experience a professional clinical environment and be treated with compassion and respect.

Study doctors will closely watch participants’ blood levels throughout the study, and may adjust or lower their daily pills based on strict safety rules to protect participant health. The study team will explain everything in detail so potential participants can make an informed decision.

No, there is no cost to participate. For qualified participants who choose to be in this study, the study  drug will be provided at no cost. There will be no charge for any tests, examinations, or visits done as part of this study. 

Participants may be reimbursed for travel costs and out of pocket expenses or these costs may be covered directly. They may also receive compensation for their time and effort.

In any clinical study for a new treatment, there are potential risks, such as side effects of the study drug  or risks from the study activities. The study staff will explain these potential risks before participants decide whether to participate, and address any concerns.

No. Before a potential participant decides whether to take part in the study, the study staff will review the informed consent form with them and answer any questions. Once the consent form has been signed by the participant, the screening period of the study begins. During this period, the staff will review medical history and conduct any relevant assessments. Participants who meet all of the study criteria will be invited to participate

Yes. Participation in clinical trials is entirely voluntary. Even if a participant is already involved in a study, they may change their mind at any time, for any reason.

If you are interested in learning more, please contact us at any time. You may email us at help@clinicalenrollment.com.