Frequently Asked Questions

Study Specific Questions

Who can participate in this clinical research study?

To participate in this study, you or a loved one must:

  • Be 18 to 65 years old, inclusive
  • Meet liver function criteria based on the study group

There are additional criteria that are reviewed by the study team during your first appointment.

You will meet with a study coordinator at a study site location closest to you. You will learn more about the research study and the benefits and risks of participation.

The study coordinator or study doctor will review the Informed Consent Form with you. You will have the chance to ask any questions about this form, and sign once comfortable and willing to participate in the study. Different procedures will be performed to confirm that you qualify for the clinical study.

MM120 is an investigational, orally disintegrating tablet containing LSD D-tartrate. It is being studied for its pharmacokinetics and effects on individuals with abnormal liver impairment.

All participants who are eligible and successfully enroll in this study will take part for up to approximately 44 days. During this time, you’ll begin with a screening period of up to 35 days to determine eligibility. If eligible, you’ll stay at the research clinic for about 4 days, where you will receive the study medication and be closely monitored by trained medical staff. After leaving the clinic, a member of the study team will check in with you by phone around Day 6, and you’ll return for a final in-person visit around Day 9. All study-related care is provided at no cost, and medical staff will support you throughout your participation.

The study centers are located throughout the United States. This website is enrolling for one specific location. Please see the study location section for details.

You do not have to stop taking your medication unless you are advised to do so by your physician.

No, there will be no cost to you for the study therapy or study procedures.

No, health insurance is not a requirement to participate in this study. If you need treatment or care outside of the study, health insurance may be required.

Questions About Clinical Research Studies

What is a clinical trial?

Clinical trials, also known as clinical studies or research studies, are conducted by doctors and researchers to see if new medications, devices, or treatments are safe and effective before being approved for use by the public. Participation in a clinical trial is completely confidential and will be protected just like any other medical information.

Research studies are used to test new medications and devices for safety, tolerability, and effectiveness before they are approved for use by the public.

All research studies require that doctors and/or researchers give interested participants complete and accurate information about the risks, benefits, and activities of a research study. Interested participants will sign an Informed Consent Form prior to enrolling in the study. This form shows that a participant understands what will happen during the study and that they can leave the study at any time.