Find a Clinical Trial
Apollo Pact does not conduct or enroll participants in clinical trials directly. To find current studies of psychedelic therapies, search the U.S. government's public clinical trials registry at clinicaltrials.gov.
You can search by condition, location, and trial phase. Each listing includes eligibility criteria and contact information for the study's research team.
Apollo Pact provides general educational information about clinical trials and does not recommend, screen for, or facilitate enrollment in any specific trial. For questions about eligibility or enrollment, contact the trial's research team directly. Have general questions about how clinical trials work? Contact us and we'll help point you in the right direction.
Your Rights as a Research Participant
At Apollo Pact, we believe people who participate in clinical research — especially psychedelic studies — deserve to be treated as partners in the future of medicine, not just subjects.
As a research participant, you have the right to:
Be treated with respect and dignity throughout every stage of a study.
Understand what you're agreeing to — the study's purpose, what's required of you, and its risks and benefits, in plain language. If a study requires tapering or stopping any medication, you have the right to a clear plan, timeline, and support before consenting.
Make a free, informed choice. No one may use pressure, coercion, or fear of losing care to obtain your consent — and you may say no.
Ask questions and get honest answers, at any point before, during, or after a study.
Know your alternatives. A study should never be presented as your only option.
Know your study was independently reviewed by an Institutional Review Board (IRB) — an independent ethics committee. You can ask who reviewed it and how to contact them.
Have your privacy protected, in accordance with applicable law, including knowing who accesses your data and how it's used.
Receive copies of everything you sign, including your informed consent form.
Know what happens if you're hurt — whether treatment or compensation is available for research-related injury.
Withdraw at any time, without penalty and without needing to explain why.
Speak up. If something feels wrong, you have the right to report it to the study's IRB or sponsor, free from retaliation, which is prohibited by federal regulation. Apollo Pact is not affiliated with any study's IRB or sponsor, is not a party to your consent agreement, and does not investigate, mediate, or resolve individual complaints. If you're unsure who to contact, email us at hello@apollopact.org and we will help you identify the right contact — we cannot act on your behalf.
Know how your participation contributes, and ask about access to study findings once available.
Apollo Pact is a nonprofit patient advocacy organization. This page is provided for general educational purposes only and does not constitute legal or medical advice, and does not create any advisory, representative, or fiduciary relationship between Apollo Pact and any reader. Apollo Pact is not a party to, and has no authority over, any specific clinical trial, its IRB, or its sponsor. For study-specific questions — including questions about your rights, consent, or a concern about a study — contact your research team or IRB directly.
If you're not sure how to find the right contact, email us at hello@apollopact.org and we can help point you in the right direction.