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Clinical Focus

Clinical Trials Digital Studies

Clinical Trials

If you are interested in participating in a clinical trial, please click on the links below in the Clinical Trial List to find trial sites near you that are open for public enrollment. Additionally, you may sign up for MindMed’s email list to get information about upcoming clinical trials.

Clinical Trial List

TRIAL NAME
Status
Location
MMED008: A Dose-Finding Study of MM-120 for the Treatment of Anxiety Symptoms
Completed
USA (20 Sites)
MMED007: Safety and Efficacy of Low Dose MM-120 for ADHD Proof of Concept Trial
Completed
Maastricht, Netherlands & Basel, Switzerland
An Open-label, Single Ascending Oral Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MM-402 in Healthy Subjects
Completed
Manchester, UK
A Study to Assess 18-Methoxycoronaridine (18-MC HCl) in Healthy Volunteers
Completed
Perth, Australia

Digital Medicine Studies

STUDY NAME
Status
Location
MM-061302: Quantifying the Processes and Events of Psychotherapy at Scale
Completed
New York, NY, USA
MSMS Program - Studies to Evaluate Participant Data in Consciousness Altering Therapeutic Sessions
Actively Recruiting, Invitation Only
Multiple Locations, Worldwide
MMED-D001: Anxiety Digital Diagnoses for Precision PsychiaTry (ADDAPT): A Natural History Study
Completed
USA (Decentralized)

Additional Resources

Participants

Visit clinicaltrials.gov to find clinical trials near you. This site is a database of privately and publicly funded clinical studies conducted around the world. Here you can find trials that are actively recruiting for different indications as well as the inclusion and exclusion criteria for different trials. You also have certain rights as a participant in a research study or clinical trial. See the Bill of Rights below for a list of these rights as well as links that provide additional information related to participant safety and research ethics.

Bill of Rights for Research Participants
As a participant in a research study, you have the right:

  1. To have enough time to decide whether or not to be in the research study and to make that decision without any pressure from the people who are conducting the research.
  2. To refuse to be in the study at all, and to stop participating at any time after you begin the study.
  3. To be told what the study is trying to find out, what will happen to you, and what you will be asked to do if you are in the study.
  4. To be told about the reasonably foreseeable risks of being in the study.
  5. To be told about the possible benefits of being in the study.
  6. To be told whether there are any costs associated with being in the study and whether you will be compensated for participating in the study.
  7. To be told who will have access to information collected about you, and how your confidentiality will be protected.
  8. To be told whom to contact with questions about the research, about research-related injury, and about your rights as a research subject.
  9. To be told about the other non-research treatment choices you have, if the study involves treatment or therapy.
  10. To be told where treatment is available should you have a research-related injury, and who will pay for research-related treatment.

Additional resources regarding the rights of research participants can be found at the following links:

Regulations to Protect Research Volunteers
Declaration of Helsinki
The Belmont Report
Inside Clinical Trials: Testing Medical Products in People

Suicide Prevention and Crisis Resources

If you are in the UNITED STATES and you or someone you know is experiencing a crisis or is in need of support, please call the 24/7 National Suicide Prevention Lifeline at 1-800-273-TALK (8255) or text HELLO to the 24/7 Crisis Text Line at 741741. You can also visit the Suicide Prevention Lifeline website.

For INTERNATIONAL crisis resources and hotlines, please visit findahelpline.com and search for resources available in your location.

If you or someone you know is experiencing a medical, mental health, or other emergency, please contact 911 or your region’s designated emergency number or proceed to your nearest emergency department.

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